{"title":"Cell Signaling and Neuroscience","description":"\u003cp\u003e\u003cstrong\u003eCell Signaling and Neuroscience\u003c\/strong\u003e — menghimpun senyawa acuan untuk riset jalur sinyal sel, mencakup sinyal kalsium, kinase dan fosfatase, lipid sinyal, sitokin, hormon, serta bahan uji untuk neurosains dan stres oksidatif. Kategori ini menyediakan modulator dan inhibitor yang menjadi alat bantu penelitian mekanisme sel.\u003c\/p\u003e\u003cp\u003eCell Signaling and Neuroscience dipakai peneliti untuk mempelajari jalur kinase\/fosfatase dengan inhibitor selektif, mengamati sinyal kalsium intraseluler, serta meneliti neurotransmiter dan reseptornya pada model eksperimen saraf. Senyawa dalam kategori ini juga menjadi bahan uji in vitro untuk studi stres oksidatif dan interaksi hormon-reseptor dalam riset biologi sel dan farmakologi molekuler.\u003c\/p\u003e\u003cp\u003eContoh produk dalam koleksi ini: \u003ca href=\"\/en\/products\/tci2510a0282407\"\u003eTCI A0282 56-12-2 4-Aminobutyric Acid\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b552012169\"\u003eTCI B5520 714971-09-2 BMS-599626\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c230217033\"\u003eTCI C2302 458-37-7 Curcumin (Synthetic)\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b559212263\"\u003eTCI B5592 132-17-2 Benztropine Mesylate\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510a0116186\"\u003eTCI A0116 1866-15-5 Acetylthiocholine Iodide\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b571612436\"\u003eTCI B5716 280744-09-4 SB 216763\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510a0305449\"\u003eTCI A0305 62-31-7 3-Hydroxytyramine Hydrochloride\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b576212495\"\u003eTCI B5762 472981-92-3 SB-366791\u003c\/a\u003e.\u003c\/p\u003e\u003cp\u003ePerhatikan selektivitas target senyawa (misalnya spesifisitas terhadap kinase tertentu), kemurnian, dan bentuk garam atau hidrat yang memengaruhi kelarutan dalam pelarut uji. Seluruh produk merupakan produk asli Tokyo Chemical Industry (TCI) Jepang, dengan kemurnian, kemasan, dan kondisi penyimpanan tercantum pada halaman masing-masing item.\u003c\/p\u003e\u003cp\u003eKategori lain yang sejajar di bawah Biologi Sel, sering dipakai bersamaan dalam satu alur kerja laboratorium:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-nutrition-research\"\u003eNutrition Research\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-cancer-research\"\u003eCancer Research\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-immune-system-inflammation-allergy-research\"\u003eImmune System, Inflammation, Allergy Research\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-bioactive-small-molecules\"\u003eBioactive Small Molecules\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-metabolomics\"\u003eMetabolomics\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-stem-cell-biology\"\u003eStem Cell Biology\u003c\/a\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eKoleksi ini masih terbagi menjadi 6 kelompok yang lebih spesifik:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-cytokines-growth-factors-and-hormones\"\u003eCytokines, Growth Factors and Hormones\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-kinase-phosphatase-biology\"\u003eKinase\/Phosphatase Biology\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-neuroscience\"\u003eNeuroscience\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-oxidative-stress\"\u003eOxidative Stress\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-lipids-in-cell-signaling\"\u003eLipids in Cell Signaling\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-calcium-signaling\"\u003eCalcium Signaling\u003c\/a\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eKembali ke \u003ca href=\"\/en\/collections\/biologi-sel\"\u003eBiologi Sel\u003c\/a\u003e. Untuk pengadaan volume besar, kemasan khusus, atau grade tertentu, hubungi tim AMI Scientific — distributor resmi TCI Japan di Indonesia — untuk pengecekan ketersediaan dan lead time langsung ke Jepang.\u003c\/p\u003e","products":[{"product_id":"tci2510b552012169","title":"TCI B5520 714971-09-2 BMS-599626","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBMS-599626 (CAS 714971-09-2) is a research-grade compound supplied by TCI, known as a selective kinase inhibitor used in laboratory studies of HER-related cell signaling pathways. It is commonly applied in oncology research, including in vitro and in vivo assays investigating tumor growth and drug resistance mechanisms. The product is available in 10 mg and 50 mg packaging for pharmaceutical and biomedical research purposes.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"10mg","offer_id":48085885026522,"sku":"TCI2510B552012169","price":3358000.0,"currency_code":"IDR","in_stock":true},{"title":"50mg","offer_id":48085885059290,"sku":"TCI2510B552012170","price":11661000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5520.jpg?v=1771058686"},{"product_id":"tci2510b559212263","title":"TCI B5592 132-17-2 Benztropine Mesylate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBenztropine Mesylate is a chemical compound widely used in pharmacological and biochemical research. It serves as a key reagent in experimental studies focused on anticholinergic effects and their impact on the central nervous system. This compound is essential for researchers aiming to understand the mechanisms of neurological disorders and the efficacy of neuropharmacological treatments. Its role in laboratory settings is critical for advancing knowledge in drug development and therapeutic applications.\u003c\/p\u003e\n\u003cp\u003eThe compound is known for its chemical stability and good solubility in organic solvents, making it highly suitable for a variety of chemical reactions. These properties ensure consistent performance in experimental protocols, contributing to reliable and reproducible results. Additionally, its thermal stability allows for ease of storage and use under varying laboratory conditions, enhancing its versatility in research applications.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Benztropine Mesylate is extensively used in pharmacological research across educational institutions and research organizations. It is a preferred choice for studying the mechanisms of antiparkinson drugs and their effects on neural systems. Researchers rely on its quality and reliability to conduct accurate and meaningful experiments in the field of neuropharmacology.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eParkinson’s Disease Research – This compound is used to study the effects of antiparkinson drugs on neural pathways and motor function.\u003c\/li\u003e\n\u003cli\u003eAnticholinergic Effect Testing – It helps in evaluating the impact of anticholinergic agents on the central nervous system and peripheral tissues.\u003c\/li\u003e\n\u003cli\u003eNeuropharmacological Studies – It is essential for investigating the pharmacodynamics and pharmacokinetics of neuroactive compounds.\u003c\/li\u003e\n\u003cli\u003eDrug Development Protocols – Its use supports the screening and evaluation of potential therapeutic agents for neurological disorders.\u003c\/li\u003e\n\u003cli\u003eClinical Trial Simulations – It aids in creating controlled environments to assess drug interactions and therapeutic outcomes in preclinical settings.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS Number: 132-17-2\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Pharmaceutical Research Reagents\u003c\/li\u003e\n\u003cli\u003ePack Sizes: Available in various quantities as per standard reagent packaging\u003c\/li\u003e\n\u003cli\u003ePhysical Form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage Note: Store in a cool, dry place away from direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eBenztropine Mesylate should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to keep the compound in airtight containers to avoid moisture exposure, which could affect its solubility and potency. Laboratory personnel should handle the material with care, using appropriate personal protective equipment such as gloves and safety goggles. The compound is non-hazardous under normal conditions but should be handled in a well-ventilated area to minimize inhalation risks. Proper labeling and storage practices ensure the safety of both the material and the laboratory environment.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48085889614042,"sku":"TCI2510B559212263","price":2802000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085889646810,"sku":"TCI2510B559212264","price":9793000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5592.jpg?v=1769180200"},{"product_id":"tci2510b571612436","title":"TCI B5716 280744-09-4 SB 216763","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B5716, with the CAS number 280744-09-4, is a chemical compound widely used in life science research, particularly in the fields of cell biology and neuroscience. This compound serves as a reagent in various experimental settings, enabling scientists to investigate cellular signaling mechanisms and neurological activities. In laboratory environments, it functions as a tool to modulate specific signaling pathways within cells, offering insights into complex biological responses. Its role is essential for understanding how cells react to external stimuli and how these responses are regulated at the molecular level.\u003c\/p\u003e\n\u003cp\u003eThe compound is preferred due to its chemical stability and high purity, ensuring consistent and reliable experimental outcomes. Its ability to specifically interact with target proteins minimizes interference from other compounds, enhancing the accuracy of research findings. These properties make it a trusted choice for researchers who require precision and reproducibility in their experiments. Additionally, its compatibility with a wide range of experimental conditions allows for flexibility in laboratory applications.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, TCI B5716 is commonly used in studies related to neurodegenerative diseases, drug development, and the investigation of cellular responses to external stimuli. It is a vital component in research aimed at uncovering the underlying mechanisms of biological processes, contributing to advancements in both basic and applied scientific research.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eNeurodegenerative disease research benefits from TCI B5716 as it aids in studying the molecular pathways involved in conditions like Alzheimer’s and Parkinson’s.\u003c\/li\u003e\n\u003cli\u003eDrug development projects utilize this compound to test the effects of potential therapeutics on specific cellular signaling pathways.\u003c\/li\u003e\n\u003cli\u003eCellular response studies rely on TCI B5716 to examine how cells react to various external stimuli, providing insights into physiological and pathological processes.\u003c\/li\u003e\n\u003cli\u003eNeuroscience experiments use this compound to investigate the role of specific signaling molecules in neural function and disease progression.\u003c\/li\u003e\n\u003cli\u003eBiochemical assays incorporate TCI B5716 to assess its interaction with target proteins, supporting the validation of molecular mechanisms in biological systems.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 280744-09-4\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Cell Biology \u0026gt; Cell Signaling and Neuroscience\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eTCI B5716 should be stored in a cool, dry place, away from direct sunlight and sources of heat. It is recommended to keep the compound in a tightly sealed container to prevent contamination and maintain its chemical integrity. Due to its stability, it does not require refrigeration under normal laboratory conditions. However, it is important to ensure that the storage area is well-ventilated to minimize exposure to airborne particles. Researchers should handle the compound with appropriate personal protective equipment, such as gloves and safety goggles, to ensure safe laboratory practices. Proper labeling of containers is also essential to prevent accidental misuse or contamination.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"10mg","offer_id":48085898952922,"sku":"TCI2510B571612436","price":3382000.0,"currency_code":"IDR","in_stock":true},{"title":"50mg","offer_id":48085898985690,"sku":"TCI2510B571612437","price":10071000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5716.jpg?v=1771058785"},{"product_id":"tci2510b576212495","title":"TCI B5762 472981-92-3 SB-366791","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eSB-366791 is a selective TRPV1 antagonist widely used in cell biology and neuroscience research to investigate calcium signaling pathways and nociceptive mechanisms. This high-purity compound from TCI is suitable for pharmacological assays, ion channel studies, and drug screening applications targeting the vanilloid receptor. It is commonly employed in preclinical research exploring therapeutic candidates for chronic pain and inflammatory conditions.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mg","offer_id":48085901377754,"sku":"TCI2510B576212495","price":5224000.0,"currency_code":"IDR","in_stock":true},{"title":"100mg","offer_id":48085901410522,"sku":"TCI2510B576212496","price":16328000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5762_0e0ba060-a1b9-4ffa-b66e-8ab32cb17e9d.jpg?v=1767863245"},{"product_id":"tci2510b577612516","title":"TCI B5776 356559-20-1 SB-525334","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eSB-525334 is a chemical compound classified under the category of enzyme substrates and inhibitors. It plays a crucial role in biochemical experiments by enabling researchers to study enzyme activity and catalytic reaction mechanisms. This compound is widely used in laboratories to assess the efficiency of specific enzymes, supporting both fundamental and applied research. Its presence in various biotechnological and pharmaceutical studies makes it an essential tool for understanding enzyme behavior and function.\u003c\/p\u003e\n\u003cp\u003eSB-525334 is preferred due to its chemical stability under specific conditions, ensuring accurate and consistent results. Its molecular structure allows for specific interactions with target enzymes, making it highly effective in enzyme mechanism studies. Additionally, it maintains its chemical activity over a defined period, offering reliability in diverse research scenarios. These properties make it a valuable reagent for researchers aiming to explore enzyme-substrate interactions and inhibition patterns.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, SB-525334 is a key component in biochemical and pharmacological research. It is commonly used in experiments related to enzyme activity, drug development, and metabolic pathway analysis. Its application extends to academic institutions and research centers, where it supports both teaching and advanced scientific investigations.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eEnzyme Kinetics Studies – SB-525334 is ideal for measuring enzyme activity and substrate turnover rates, providing precise data for kinetic analysis.\u003c\/li\u003e\n\u003cli\u003eDrug Development Research – It is used to evaluate enzyme inhibition and substrate specificity, aiding in the design of targeted pharmaceutical compounds.\u003c\/li\u003e\n\u003cli\u003eBiochemical Assays – Its stability and specificity make it suitable for standard biochemical assays that require controlled enzyme-substrate interactions.\u003c\/li\u003e\n\u003cli\u003eMetabolic Pathway Analysis – SB-525334 helps in tracing enzyme activity within metabolic pathways, supporting functional genomics and proteomics studies.\u003c\/li\u003e\n\u003cli\u003eTeaching and Training – It is commonly used in educational settings to demonstrate enzyme mechanisms and biochemical processes to students and researchers.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand – TCI\u003c\/li\u003e\n\u003cli\u003eCAS Number – 356559-20-1\u003c\/li\u003e\n\u003cli\u003eCategory – Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Enzymes, Enzyme Inhibitors, Enzyme Substrates\u003c\/li\u003e\n\u003cli\u003ePack Sizes – Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical Form – Solid or liquid, depending on formulation\u003c\/li\u003e\n\u003cli\u003eStorage Note – Store in a cool, dry place away from direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eSB-525334 should be stored in a cool, dry environment to maintain its chemical stability and activity. It is recommended to keep the compound in airtight containers to prevent moisture exposure and contamination. Proper labeling of storage containers is essential for safe handling and traceability. Laboratory personnel should wear appropriate personal protective equipment when handling the compound. Regular monitoring of storage conditions ensures the integrity of the material. Adherence to standard laboratory safety protocols minimizes risks associated with chemical exposure.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"10mg","offer_id":48085902229722,"sku":"TCI2510B577612516","price":5527000.0,"currency_code":"IDR","in_stock":true},{"title":"50mg","offer_id":48085902262490,"sku":"TCI2510B577612517","price":19938000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5776.jpg?v=1768815892"},{"product_id":"tci2510b578112521","title":"TCI B5781 133052-90-1 Bisindolylmaleimide I","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBisindolylmaleimide I is a chemical compound widely used in life sciences research, particularly in cell biology and neuroscience. It functions as a potent inhibitor of protein kinase C (PKC), a critical enzyme involved in various cellular signaling pathways. In laboratory settings, this compound is essential for controlling PKC activity and studying its role in cellular processes such as cell differentiation, apoptosis, and immune responses. Its utility spans across multiple research areas, making it a valuable tool for scientists aiming to understand complex biological mechanisms.\u003c\/p\u003e\n\u003cp\u003eThe compound is favored for its chemical stability and good solubility in organic solvents, which simplifies its use in diverse experimental protocols. Its high specificity and effectiveness in inhibiting PKC make it a preferred choice for researchers requiring precise control over enzymatic activity. This reliability ensures consistent results, which is crucial in both basic and applied research. Additionally, its well-documented properties contribute to its widespread adoption in both academic and industrial research environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Bisindolylmaleimide I is commonly used in studies related to neurodegenerative diseases, drug development, and cellular signaling mechanisms. Its relevance in local research efforts highlights its importance in advancing scientific understanding and innovation within the region. Researchers rely on this compound to achieve accurate and reproducible outcomes in their experiments.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eNeurodegenerative disease research utilizes Bisindolylmaleimide I to study the role of PKC in neuronal cell death and disease progression.\u003c\/li\u003e\n\u003cli\u003eDrug development projects employ this compound to investigate its potential as a therapeutic agent in targeting PKC-related pathways.\u003c\/li\u003e\n\u003cli\u003eCellular signaling studies benefit from its ability to modulate PKC activity, enabling the analysis of intracellular communication pathways.\u003c\/li\u003e\n\u003cli\u003eApoptosis research uses Bisindolylmaleimide I to examine how PKC inhibition affects programmed cell death mechanisms.\u003c\/li\u003e\n\u003cli\u003eImmunological studies incorporate this compound to explore its impact on immune cell signaling and response pathways.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 133052-90-1\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Cell Biology \u0026gt; Cell Signaling and Neuroscience\u003c\/li\u003e\n\u003cli\u003ePack sizes: As available from supplier\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid (as per standard product description)\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eBisindolylmaleimide I should be stored in a cool, dry environment, away from direct light to maintain its chemical stability. It is recommended to use airtight containers to prevent moisture absorption and contamination. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. Proper ventilation is essential when working with this compound to minimize exposure. It is important to store it separately from incompatible substances to avoid any potential chemical reactions. Always follow standard laboratory safety protocols when handling and storing this compound.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mg","offer_id":48085903147226,"sku":"TCI2510B578112521","price":3963000.0,"currency_code":"IDR","in_stock":true},{"title":"25mg","offer_id":48085903179994,"sku":"TCI2510B578112522","price":13880000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5781.jpg?v=1771057907"},{"product_id":"tci2510b589812669","title":"TCI B5898 193551-21-2 SB 239063","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eSB 239063 is a research compound from TCI intended for cell signaling and neuroscience studies in the laboratory. It is widely applied in cell biology, pharmacology, and neurobiology research to investigate intracellular signaling pathways and cellular response regulation. Researchers rely on this compound to explore mechanisms relevant to inflammatory and neurological conditions.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mg","offer_id":48085908914394,"sku":"TCI2510B589812669","price":4795000.0,"currency_code":"IDR","in_stock":true},{"title":"25mg","offer_id":48085908947162,"sku":"TCI2510B589812670","price":15648000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5898.jpg?v=1768815920"},{"product_id":"tci2510b605612861","title":"TCI B6056 694433-59-5 SB-505124","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6056 (SB-505124) is a selective inhibitor of TGF-β type I receptors (ALK4, ALK5, and ALK7), commonly used as a reference compound in TGF-β\/Smad signaling pathway studies. This compound is widely applied in cancer research to investigate tumor cell proliferation, metastasis, and epithelial-mesenchymal transition (EMT), as well as in developmental biology and stem cell research. It is available in 5 mg and 25 mg packaging variants, suitable for in vitro and cell-based assays.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mg","offer_id":48085917139162,"sku":"TCI2510B605612861","price":2474000.0,"currency_code":"IDR","in_stock":true},{"title":"25mg","offer_id":48085917171930,"sku":"TCI2510B605612862","price":8834000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6056.jpg?v=1768815966"},{"product_id":"tci2510b606812876","title":"TCI B6068 119139-23-0 Bisindolylmaleimide IV","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBisindolylmaleimide IV (TCI B6068) is a chemical compound widely used in life science research, particularly in the study of cell signaling and neuroscience. As a potent inhibitor of protein kinase C (PKC), this compound plays a critical role in cellular signal transduction pathways. It is commonly utilized in laboratory settings to modulate PKC activity, enabling researchers to investigate its impact on various biological processes such as cell differentiation, apoptosis, and immune responses. Its importance lies in its ability to provide insights into the molecular mechanisms underlying these complex biological functions.\u003c\/p\u003e\n\u003cp\u003eThe compound is valued for its chemical stability and high solubility in organic solvents like DMSO, making it easy to dissolve and incorporate into experimental protocols. Its strong affinity for its target enzyme ensures high efficacy in inhibiting PKC, which is essential for studies requiring precise modulation of signaling pathways. These properties make it a reliable and effective tool for researchers aiming to explore the role of PKC in both normal and pathological conditions.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Bisindolylmaleimide IV is a key reagent in biomedical, pharmacological, and neurobiological research. Its use supports the development of new therapeutic strategies and the understanding of disease mechanisms. Due to its reliability and effectiveness, it is a preferred choice for scientists working in these fields.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eCell Signaling Studies: This compound is ideal for investigating the role of PKC in intracellular signaling pathways, allowing researchers to analyze how its inhibition affects cellular responses.\u003c\/li\u003e\n\u003cli\u003eNeurobiological Research: It is used to study the impact of PKC inhibition on neuronal function, helping to uncover mechanisms related to neurodegenerative diseases and synaptic plasticity.\u003c\/li\u003e\n\u003cli\u003eApoptosis and Cell Differentiation: Its ability to modulate PKC activity makes it suitable for experiments examining the role of this enzyme in programmed cell death and developmental processes.\u003c\/li\u003e\n\u003cli\u003eImmunological Investigations: Researchers use it to study how PKC inhibition influences immune cell activation and response, contributing to the understanding of immune-related disorders.\u003c\/li\u003e\n\u003cli\u003eDrug Development: It serves as a tool in the development of pharmaceutical compounds targeting PKC, aiding in the design of potential therapeutic agents.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS Number: 119139-23-0\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Cell Biology \u0026gt; Cell Signaling and Neuroscience\u003c\/li\u003e\n\u003cli\u003ePack Sizes: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003ePhysical Form: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003eStorage Note: Store in a cool, dry place away from light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eBisindolylmaleimide IV should be stored in a cool, dry place, away from direct light to maintain its chemical stability. It is recommended to use airtight containers to prevent moisture absorption, which could affect its potency. Due to its potential reactivity, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles. In laboratory settings, it is important to ensure proper ventilation when working with this compound. It should not be disposed of in drains or landfills without following local regulations for chemical waste. Proper labeling and storage are essential to ensure safety and maintain the integrity of the compound for research use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"50mg","offer_id":48085917663450,"sku":"TCI2510B606812876","price":1439000.0,"currency_code":"IDR","in_stock":true},{"title":"250mg","offer_id":48085917696218,"sku":"TCI2510B606812877","price":4947000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6068.jpg?v=1768815971"},{"product_id":"tci2510b614312963","title":"TCI B6143 113963-68-1 Bisindolylmaleimide V","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBisindolylmaleimide V is a small organic compound belonging to the bisindolylmaleimide family, a class of molecules built around a maleimide core bearing two indole groups attached at the 3 and 4 positions. This family of compounds is widely recognised in cell biology research, particularly in studies of signalling pathways that involve protein kinase C. In molecular biology and pharmacology laboratories, compounds in this group serve as chemical tools for examining how cells relay signals from the cell surface toward the nucleus, and Bisindolylmaleimide V in particular is frequently employed as a structural comparison compound within such experimental series.\u003c\/p\u003e\n\u003cp\u003eThe property that leads researchers to select this compound is its very close structural resemblance to other members of the bisindolylmaleimide series. Because of that similarity, it can be paired with related analogues within a single experimental design in order to distinguish effects that genuinely arise from kinase inhibition from effects that arise instead from the physicochemical character of the molecular scaffold itself. This ability to separate a specific biochemical response from a general scaffold-driven response is what gives the compound its value as a reference material in carefully controlled signalling studies.\u003c\/p\u003e\n\u003cp\u003eAs a small molecule with relatively lipophilic character, this compound is generally dissolved in dimethyl sulfoxide before being diluted into culture medium — a working pattern already very familiar to cell culture laboratories in Indonesia. University research laboratories, molecular biology facilities, and pharmacology groups working on cell signalling typically handle the compound in this manner, preparing concentrated stock solutions that are then introduced into treatment experiments on cultured cells.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eProtein kinase C signalling studies, where the compound serves as a chemical tool for probing how signals initiated at the cell surface are transmitted through the cytoplasm toward the nucleus.\u003c\/li\u003e\n\u003cli\u003eStructural comparison experiments, in which this compound is paired with other bisindolylmaleimide analogues so that scaffold-related effects can be separated from genuine kinase-inhibition effects.\u003c\/li\u003e\n\u003cli\u003eCell biology research on signal transduction, where small-molecule modulators are applied to cultured cells to examine downstream cellular responses under controlled treatment conditions.\u003c\/li\u003e\n\u003cli\u003ePharmacology investigations of compound specificity, since the close structural relationship within the bisindolylmaleimide series supports rational experimental designs that test whether an observed response is target-specific.\u003c\/li\u003e\n\u003cli\u003eNeuroscience-oriented cell signalling work, where members of this compound family are used to interrogate kinase-dependent pathways in neuronal and other cultured cell models under laboratory conditions.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eProduct code: B6143\u003c\/li\u003e\n\u003cli\u003eCAS number: 113963-68-1\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Cell Biology \u0026gt; Cell Signaling and Neuroscience\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the research-scale pack sizes listed by the manufacturer for this catalogue item\u003c\/li\u003e\n\u003cli\u003eStorage: store according to the manufacturer's stated conditions on the product label and accompanying documentation\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the compound in its original tightly closed container, protected from moisture and light, and follow the storage conditions stated by the manufacturer on the product label and safety data sheet. Amber glass vials are suitable for both the solid material and any prepared stock solution. Because the compound is typically dissolved in dimethyl sulfoxide before dilution into culture medium, prepare stock solutions in a clean working area, label aliquots clearly, and avoid repeated freeze-thaw cycles where practicable. Handle the material with gloves, a laboratory coat, and eye protection, weigh the solid in a well-ventilated enclosure to limit inhalation of fine powder, and dispose of residues and contaminated consumables through the laboratory's established chemical waste stream.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"10mg","offer_id":48085921792218,"sku":"TCI2510B614312963","price":733000.0,"currency_code":"IDR","in_stock":true},{"title":"50mg","offer_id":48085921824986,"sku":"TCI2510B614312964","price":2524000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6143.jpg?v=1768815994"},{"product_id":"tci2510b648513387","title":"TCI B6485 149-64-4 Buscopan","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6485, Buscopan or hyoscine butylbromide (CAS 149-64-4), is a quaternary ammonium derivative of a tropane alkaloid and a well-known muscarinic receptor antagonist. Its high polarity and good aqueous solubility make it convenient for preparing stock solutions in in vitro pharmacology work and for use as an analytical reference standard. Common laboratory applications include HPLC and LC-MS method development, smooth muscle contraction studies, and natural product chemistry teaching. AMI Scientific supplies this TCI product in 1 g and 5 g packs strictly for research and analytical purposes, not for human diagnostic or therapeutic use.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSissons et al. (1991). The ocular effects of hyoscine-n-butylbromide (“Buscopan”) in radiological practice. \u003cem\u003eThe British Journal of Radiology\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1259\/0007-1285-64-763-584\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1259\/0007-1285-64-763-584\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eZitvast (2023). Buscopan tegen Reutelen. \u003cem\u003eNursing\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1007\/s41193-023-0736-0\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1007\/s41193-023-0736-0\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003e(1992). A comparison of intravenous and intramuscular buscopan for barium meal examinations. \u003cem\u003eClinical Radiology\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/s0009-9260(05)80810-4\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/s0009-9260(05)80810-4\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085942894810,"sku":"TCI2510B648513387","price":1742000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085942927578,"sku":"TCI2510B648513388","price":5906000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6485.jpg?v=1768204505"},{"product_id":"tci2510b654413470","title":"TCI B6544 61-75-6 Bretylium Tosylate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBretylium tosylate (CAS 61-75-6) is a quaternary ammonium compound long recognised in the literature as an adrenergic neuron blocker that interferes with norepinephrine release from sympathetic nerve terminals. It is widely used as a reference pharmacological tool in cardiovascular and autonomic nervous system research, including studies of antiarrhythmic mechanisms and cardiac repolarisation. The material is supplied strictly for research and experimental use and is not intended for human diagnostic or therapeutic application. AMI Scientific offers a 25 mg pack size suitable for isolated tissue experiments and cell-based assays.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eFallen (2000). Bretylium Tosylate (UDATE—2000). \u003cem\u003eCardiac Electrophysiology Review\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1023\/a:1026583112967\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1023\/a:1026583112967\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eMuhammad et al. (1999). The effect of bretylium tosylate on ECG-guided pericardiocentesis. \u003cem\u003eAnnals of Emergency Medicine\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/s0196-0644(99)80198-x\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/s0196-0644(99)80198-x\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eDeBehnke (1991). Effects of bretylium tosylate during experimental cardiac arrest. \u003cem\u003eThe American Journal of Emergency Medicine\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/0735-6757(91)90064-q\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/0735-6757(91)90064-q\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mg","offer_id":48085946302682,"sku":"TCI2510B654413470","price":5527000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6544.jpg?v=1768204511"},{"product_id":"tci2510b672813655","title":"TCI B6728 606143-89-9 MEK 162","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eMEK 162 is a small-molecule inhibitor that targets MEK1 and MEK2, the key kinases within the RAS–RAF–MEK–ERK signalling pathway. In cell biology and molecular pharmacology laboratories, this compound is used as a research tool to selectively block that pathway, allowing researchers to observe the biological consequences that follow when proliferative signal transmission is interrupted at a defined point. The MAPK pathway is among the most extensively studied signalling cascades because of its role in regulating cell growth, differentiation, and survival, which makes a reliable pathway inhibitor a frequently requested reagent in signalling work.\u003c\/p\u003e\n\u003cp\u003eThe characteristics that make this compound a widely chosen option are its selectivity toward MEK1\/2 together with its ability to act at low concentrations in cell culture, so that the observed effects can be attributed to inhibition of the intended pathway with greater confidence. Inhibition of MEK suppresses downstream ERK phosphorylation, and this readout is straightforward to monitor using standard immunoblot techniques with phospho-ERK antibodies. The compound is also soluble in dimethyl sulfoxide, so it is easily prepared as a concentrated stock solution and diluted into culture medium across whatever concentration range an experiment requires.\u003c\/p\u003e\n\u003cp\u003eIn Indonesia, this compound is typically used in university and institutional research laboratories working on cell biology, molecular pharmacology, and cell signalling. It generally appears in experiments where a defined pathway inhibitor is needed to establish whether an observed cellular response depends on MAPK signalling. Because the material is supplied by TCI and handled as a research-grade reagent, it is ordered in the small quantities appropriate to cell culture work, prepared as DMSO stocks, and applied across the dilution series a given study calls for.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSelective inhibition of MAPK signalling in cultured cells, where its selectivity toward MEK1\/2 lets researchers interrupt the RAS–RAF–MEK–ERK cascade at one defined node rather than broadly suppressing kinase activity.\u003c\/li\u003e\n\u003cli\u003ePhospho-ERK immunoblot studies, because MEK inhibition suppresses downstream ERK phosphorylation and that change is readily detected with standard phospho-ERK antibodies in routine Western blot workflows.\u003c\/li\u003e\n\u003cli\u003eCell proliferation and growth studies, since the MAPK pathway governs proliferative signalling and blocking it reveals how strongly a given cell population depends on that cascade for growth.\u003c\/li\u003e\n\u003cli\u003eCell differentiation and survival research, where the compound allows investigators to test whether differentiation or survival phenotypes observed in culture require active signalling through MEK1 and MEK2.\u003c\/li\u003e\n\u003cli\u003eMolecular pharmacology and pathway-dependency screening, as its activity at low concentrations in cell culture supports dose-response designs that link an observed biological effect to inhibition of the target pathway.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 606143-89-9\u003c\/li\u003e\n\u003cli\u003eProduct code: B6728\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Cell Biology \u0026gt; Cell Signaling and Neuroscience\u003c\/li\u003e\n\u003cli\u003eSolubility: soluble in dimethyl sulfoxide (DMSO), suitable for preparation of concentrated stock solutions\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in research-scale quantities as supplied by the manufacturer; please confirm the packaging option required\u003c\/li\u003e\n\u003cli\u003eStorage: store according to the manufacturer's instructions on the product label and certificate of analysis\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the compound according to the storage conditions stated by the manufacturer on the product label, keeping the container tightly closed and protected from moisture. Stock solutions prepared in dimethyl sulfoxide should be kept in tightly sealed, clearly labelled vials, ideally divided into single-use aliquots to limit repeated freeze-thaw cycles and reduce moisture uptake by the solvent. Handle the material in a well-ventilated area or a fume hood, and use gloves, safety glasses, and a laboratory coat when weighing the solid or preparing solutions. Dilution into culture medium should be carried out under aseptic conditions in a biological safety cabinet. As with any research-grade compound intended solely for laboratory use, consult the safety data sheet before handling, avoid contact with skin and eyes, and dispose of unused material and contaminated consumables through the laboratory's chemical waste procedure.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48085954035930,"sku":"TCI2510B672813655","price":6840000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6728.jpg?v=1768816096"},{"product_id":"tci2510b680313719","title":"TCI B6803 501437-28-1 BI-D 1870","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6803 BI-D 1870 (CAS 501437-28-1) is a widely used small-molecule inhibitor of p90 ribosomal S6 kinase (RSK), acting on the N-terminal kinase domain. It serves as a standard pharmacological tool for dissecting the RAS–ERK–RSK axis in cell signalling and neuroscience research. Typical workflows involve preparing a DMSO stock solution, diluting into culture medium, and monitoring downstream substrate phosphorylation, proliferation, or translational output. Available in 5 mg and 25 mg packs, the compound should be stored cold, protected from light and moisture, and aliquoted to avoid repeated freeze–thaw cycles.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003e(1991). Pawnee passage, 1870-1875. \u003cem\u003eChoice Reviews Online\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.5860\/choice.28-5271\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.5860\/choice.28-5271\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003e(1991). Making America corporate, 1870-1920. \u003cem\u003eChoice Reviews Online\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.5860\/choice.28-3970\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.5860\/choice.28-3970\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003e(1991). The Symbolist generation, 1870-1910. \u003cem\u003eChoice Reviews Online\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.5860\/choice.28-5510\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.5860\/choice.28-5510\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mg","offer_id":50506866262234,"sku":"TCI2510B680313719","price":2297000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6803.jpg?v=1768816104"},{"product_id":"tci2510c001013918","title":"TCI C0010 464-49-3 (+)-Camphor","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0010 (+)-Camphor, CAS 464-49-3, is an enantiomerically defined bicyclic ketone widely used as a chiral pool starting material. Its rigid bornane framework provides a reliable steric environment for asymmetric induction, making it valuable for preparing chiral auxiliaries, ligands, and resolving agents. The reactive C-2 ketone allows straightforward conversion into oximes, imines, alcohols, and other functionalised derivatives. AMI Scientific supplies this TCI product in 25 g and 500 g pack sizes for both method development and routine synthetic work.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003e(2016). Camphor. \u003cem\u003eReactions Weekly\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1007\/s40278-016-16081-z\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1007\/s40278-016-16081-z\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eSahana et al. (2012). Camphor poisoning. \u003cem\u003eIndian Pediatrics\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1007\/s13312-012-0174-6\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1007\/s13312-012-0174-6\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eMONEY (1996). ChemInform Abstract: Remote Functionalization of Camphor: Application to Natural Product Synthesis. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199649291\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199649291\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085965701338,"sku":"TCI2510C001013918","price":455000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085965734106,"sku":"TCI2510C001013919","price":2273000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0010.jpg?v=1767094541"},{"product_id":"tci2510c001813936","title":"TCI C0018 2219-31-0 L-Canavanine Sulfate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0018 L-Canavanine Sulfate, CAS 2219-31-0, is a non-proteinogenic amino acid found naturally in leguminous plants and supplied here as its sulfate salt. Structurally it is a close analogue of L-arginine, which allows it to compete with arginine in a range of biological processes. This makes it a useful probe in biochemical research, peptide chemistry, plant metabolism studies, and investigations of natural plant defence compounds. AMI Scientific offers this TCI product in a 100 mg pack size, appropriate for laboratory-scale experiments requiring low working concentrations.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48085966356698,"sku":"TCI2510C001813936","price":2449000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0018.jpg?v=1771058480"},{"product_id":"tci2510c031514370","title":"TCI C0315 83-44-3 Deoxycholic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0315 Deoxycholic Acid (CAS 83-44-3) is a naturally occurring secondary bile acid widely used as a biochemical reagent. Its amphiphilic steroid structure allows it to act as a biological surfactant for membrane solubilization, micelle formation, and lipid emulsification studies. TCI lists it under animal disease model preparation, and it is also a common starting material in bile acid and steroid chemistry research. AMI Scientific supplies this reagent in 25 g and 100 g packs; store it dry, tightly closed, and follow the manufacturer's safety data sheet.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eJegasothy (2018). Deoxycholic Acid Injections for Bra-Line Lipolysis. \u003cem\u003eDermatologic Surgery\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1097\/dss.0000000000001311\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1097\/dss.0000000000001311\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003e(2018). Deoxycholic-acid. \u003cem\u003eReactions Weekly\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1007\/s40278-018-48224-z\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1007\/s40278-018-48224-z\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eSachdev et al. (2018). Deoxycholic Acid–Induced Skin Necrosis: Prevention and Management. \u003cem\u003eDermatologic Surgery\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1097\/dss.0000000000001384\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1097\/dss.0000000000001384\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085989458138,"sku":"TCI2510C031514370","price":1541000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48085989490906,"sku":"TCI2510C031514371","price":4266000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0315.jpg?v=1767095019"},{"product_id":"tci2510c031614372","title":"TCI C0316 302-95-4 Sodium Deoxycholate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0316 Sodium Deoxycholate (CAS 302-95-4) is the sodium salt of deoxycholic acid and functions as a mild anionic detergent with good aqueous solubility. It is a standard component of cell lysis buffers, membrane protein extraction protocols, and immunoprecipitation workflows where non-specific binding must be minimized. TCI classifies it under animal disease model preparation reagents for life science research. AMI Scientific offers 25 g and 100 g packs; keep the powder tightly closed in a dry place and follow the manufacturer's safety data sheet.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eKano et al. (1991). Specific interactions between sodium deoxycholate and its water-insoluble analogues: mechanisms for premicelle and micelle formation of sodium deoxycholate. \u003cem\u003eThe Journal of Physical Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1021\/j100155a086\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1021\/j100155a086\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eKumar et al. (2024). Binary Mixed Micelles of Hexadecyltrimethylammonium Bromide–Sodium Deoxycholate and Dodecyltrimethylammonium Bromide–Sodium Deoxycholate: Thermodynamic Stabilization and Mixed Micelle Solubilization Capacity of Daidzein (Isoflavonoid). \u003cem\u003eIndustrial \u0026amp; Engineering Chemistry Research\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1021\/acs.iecr.3c04484\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1021\/acs.iecr.3c04484\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eLi et al. (1999). Aggregation Dynamics of Sodium Taurodeoxycholate and Sodium Deoxycholate. \u003cem\u003eLangmuir\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1021\/la9903705\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1021\/la9903705\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085989556442,"sku":"TCI2510C031614372","price":1566000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48085989589210,"sku":"TCI2510C031614373","price":4721000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0316.jpg?v=1768816207"},{"product_id":"tci2510c031714374","title":"TCI C0317 80-97-7 beta-Cholestanol (contains alpha-Cholestanol)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0317 beta-Cholestanol (CAS 80-97-7) is a saturated sterol closely related to cholesterol, supplied in a grade that contains alpha-cholestanol as stated in the product name. It is widely used as a structural comparator in lipid membrane research, sterol analysis, and steroid biosynthesis studies. The saturated ring system provides different packing behavior from cholesterol, which is valuable when examining membrane fluidity and ordering. AMI Scientific offers 1 g, 5 g, and 25 g packs; store the material dry, tightly closed, and protected from light per the manufacturer's instructions.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48085989621978,"sku":"TCI2510C031714374","price":1692000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085989654746,"sku":"TCI2510C031714375","price":5527000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48085989687514,"sku":"TCI2604C031794","price":481000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0317.jpg?v=1768816208"},{"product_id":"tci2510c031814376","title":"TCI C0318 57-88-5 Cholesterol (stabilized with alpha-Tocopherol)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0318 Cholesterol (CAS 57-88-5), stabilized with alpha-tocopherol, is a key sterol reagent for drug delivery system research. It is routinely used in liposome preparation, lipid nanoparticle development, and membrane biochemistry, where it modulates bilayer stability and permeability. Because cholesterol is prone to oxidation, the material should be kept tightly closed, cool, and protected from light and air. AMI Scientific offers 25 g, 100 g, and 500 g packs for research and laboratory use, in line with the manufacturer's handling instructions.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085989753050,"sku":"TCI2510C031814376","price":1263000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48085989785818,"sku":"TCI2510C031814377","price":3560000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085989818586,"sku":"TCI2510C031814378","price":12367000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0318.jpg?v=1767095027"},{"product_id":"tci2510c032414385","title":"TCI C0324 81-25-4 Cholic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0324 Cholic Acid (CAS 81-25-4) is a primary bile acid with a facially amphiphilic steroid structure that enables micelle formation and lipid solubilisation. It is widely used as a biological surfactant, as a chiral building block in supramolecular chemistry, and as a starting material for bile acid derivatives. Researchers also apply it as a reference compound in bile acid analysis and lipid metabolism studies. Supplied by Tokyo Chemical Industry in 25 g and 500 g packs for research and experimental use only, it should be stored cool, dry, and tightly closed.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003e(2016). Cholic acid. \u003cem\u003eReactions Weekly\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1007\/s40278-016-21621-4\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1007\/s40278-016-21621-4\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eDastidar (2000). Crystal structure of the inclusion complex of cholic acid with 4-aminopyridine: a novel supramolecular architecture of cholic acid. \u003cem\u003eCrystEngComm\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1039\/b001347l\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1039\/b001347l\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eLenz (2009). Relation between Cholic Acid Synthesis Rate and Faecal Radioisotope Excretion Following Oral Administration of 14 C-Cholic Acid. \u003cem\u003eDigestion\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1159\/000197998\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1159\/000197998\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085990179034,"sku":"TCI2510C032414385","price":1289000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085990211802,"sku":"TCI2510C032414386","price":14133000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0324.jpg?v=1767095031"},{"product_id":"tci2510c032514387","title":"TCI C0325 361-09-1 Sodium Cholate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0325 Sodium Cholate (CAS 361-09-1) is the sodium salt of cholic acid and functions as a water-soluble, naturally derived anionic surfactant. It is routinely used to solubilise membrane proteins, prepare liposomes and proteoliposomes, and disperse nanomaterials such as carbon nanotubes in aqueous media. In polymer and materials work it acts as an additive that modifies interfacial properties and dispersion stability. Supplied by Tokyo Chemical Industry in 25 g, 100 g, and 500 g packs, it should be kept tightly closed in a cool, dry place to prevent caking.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eWahle et al. (1996). Sodium Cholate Methanolate and Sodium Cholate 2-Propanolate. \u003cem\u003eActa Crystallographica Section C Crystal Structure Communications\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1107\/s0108270196006506\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1107\/s0108270196006506\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eSingh et al. (2020). Temperature dependent micellar behaviour of sodium cholate and sodium deoxycholate in the presence of ceftriaxone sodium: A physicochemical study. \u003cem\u003eJournal of Molecular Liquids\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.molliq.2020.113833\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.molliq.2020.113833\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eKumar et al. (2015). Volumetric, compressibility and viscometric studies on sodium cholate\/sodium deoxycholate–amino acid interactions in aqueous medium. \u003cem\u003eThermochimica Acta\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.tca.2015.02.014\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.tca.2015.02.014\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085990408410,"sku":"TCI2510C032514387","price":1642000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48085990441178,"sku":"TCI2510C032514388","price":5276000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085990473946,"sku":"TCI2510C032514389","price":17212000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0325.jpg?v=1768816214"},{"product_id":"tci2510c032914395","title":"TCI C0329 67-48-1 Choline Chloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0329 Choline Chloride (CAS 67-48-1) is a highly water-soluble quaternary ammonium salt widely used as a phase transfer catalyst in two-phase organic reactions. It is best known as a key component of deep eutectic solvents, typically combined with hydrogen bond donors such as urea, and is central to many green chemistry and electrodeposition studies. The compound also serves as a choline source in nutrition and biochemistry research. Supplied by Tokyo Chemical Industry in 25 g and 500 g packs, it is strongly hygroscopic and must be stored tightly closed in a cool, dry, moisture-free environment.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eLin et al. (2014). Henry’s constant of carbon dioxide-aqueous deep eutectic solvent (choline chloride\/ethylene glycol, choline chloride\/glycerol, choline chloride\/malonic acid) systems. \u003cem\u003eThe Journal of Chemical Thermodynamics\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.jct.2013.08.029\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.jct.2013.08.029\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eZHANG et al. (2014). Properties and applications of choline chloride\/urea and choline chloride\/glycerol. \u003cem\u003eSCIENTIA SINICA Chimica\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1360\/n032014-00001\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1360\/n032014-00001\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eAbbas et al. (2011). Anodic Dissolution of Refractory Metals in Choline Chloride Based Binary Mixtures. \u003cem\u003eECS Transactions\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1149\/1.3566089\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1149\/1.3566089\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085990703322,"sku":"TCI2510C032914395","price":505000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085990736090,"sku":"TCI2510C032914396","price":1591000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0329.jpg?v=1767095043"},{"product_id":"tci2510c035214419","title":"TCI C0352 14371-10-9 trans-Cinnamaldehyde","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003etrans-Cinnamaldehyde (TCI C0352, CAS 14371-10-9) is a conjugated aromatic aldehyde best known as the principal aroma compound of cinnamon. In the laboratory it functions as a versatile non-heterocyclic building block, offering both a reactive carbonyl group and a conjugated double bond in a single molecule. It is commonly used as a model substrate in iminium organocatalysis, Michael additions, and heterocycle construction. AMI Scientific supplies it in 25 mL and 500 mL packs, and handling in a fume hood with appropriate personal protective equipment is strongly recommended.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eGholivand et al. (2008). Simultaneous Determination of Trans-Cinnamaldehyde and Benzaldehyde in Different Real Samples by Differential Pulse Polarography and Study of Heat Stability of Trans-Cinnamaldehyde. \u003cem\u003eAnalytical Letters\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1080\/00032710802507893\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1080\/00032710802507893\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eAli et al. (2021). Trans-Cinnamaldehyde Attenuates Enterococcus faecalis Virulence and Inhibits Biofilm Formation. \u003cem\u003eAntibiotics\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.3390\/antibiotics10060702\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.3390\/antibiotics10060702\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eSwales et al. (1996). Studies on trans-cinnamaldehyde II: Mechanisms of cytotoxicity in rat isolated hepatocytes. \u003cem\u003eToxicology in Vitro\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/0887-2333(95)00105-0\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/0887-2333(95)00105-0\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48085991719130,"sku":"TCI2510C035214419","price":455000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48085991751898,"sku":"TCI2510C035214420","price":1491000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0352.jpg?v=1767095079"},{"product_id":"tci2510c038814478","title":"TCI C0388 50-22-6 Corticosterone","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0388 Corticosterone, CAS 50-22-6, is a naturally occurring glucocorticoid steroid and the principal stress hormone in rodents. It is widely used as an analytical standard for hormone quantification and as a reference ligand in glucocorticoid receptor and HPA-axis research. Laboratories also apply it as a substrate in steroid metabolism studies and for controlled glucocorticoid exposure in cell culture experiments. Offered by AMI Scientific in 100 mg, 1 g, and 5 g packs, it is intended for laboratory research use only and should be stored cool, dry, and protected from light.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eYoung (1995). Normal glucocorticoid fast feedback following chronic 50% corticosterone pellet treatment. \u003cem\u003ePsychoneuroendocrinology\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/0306-4530(95)00012-7\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/0306-4530(95)00012-7\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eHennessy (1991). Sensitization of the plasma corticosterone response to novel environments. \u003cem\u003ePhysiology \u0026amp; Behavior\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/0031-9384(91)90579-d\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/0031-9384(91)90579-d\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eJiang et al. (2019). Overexpression of SIRT1 Inhibits Corticosterone-Induced Autophagy. \u003cem\u003eNeuroscience\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.neuroscience.2019.05.035\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.neuroscience.2019.05.035\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48085995520218,"sku":"TCI2510C038814478","price":733000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48085995552986,"sku":"TCI2510C038814479","price":3584000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085995585754,"sku":"TCI2510C038814480","price":12114000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0388.jpg?v=1767095159"},{"product_id":"tci2510c038914481","title":"TCI C0389 50-04-4 Cortisone Acetate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0389 Cortisone Acetate, CAS 50-04-4, is the acetate ester of cortisone, supplied as a pharmaceutical research reagent for experimental use. It is commonly employed as a reference standard in corticosteroid analysis and as a model compound in studies of glucocorticoid signalling and anti-inflammatory mechanisms. Additional applications include enzyme studies of cortisone–cortisol interconversion and experimental formulation or stability work. AMI Scientific supplies 1 g, 5 g, and 25 g packs; the material is for laboratory research only and should be stored tightly closed in a cool, dry place away from light.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003e(2008). EXPERIMENTS WITH ACTH AND CORTISONE ACETATE ON CALVES AND GOATS. \u003cem\u003eActa Anatomica\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1159\/000142112\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1159\/000142112\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eCHURCH et al. (1999). Plasma cortisol concentrations following cortisone infusion in dogs before and after treatment with cortisone acetate. \u003cem\u003eAustralian Veterinary Journal\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1111\/j.1751-0813.1999.tb13163.x\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1111\/j.1751-0813.1999.tb13163.x\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003ePrice (2009). The Effect of Cortisone Acetate on Albino Rabbit Choroidal Mast Cells. \u003cem\u003eOphthalmic Research\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1159\/000264718\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1159\/000264718\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085995651290,"sku":"TCI2510C038914481","price":657000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085995684058,"sku":"TCI2510C038914482","price":1768000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085995716826,"sku":"TCI2510C038914483","price":5527000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0389.jpg?v=1768197104"},{"product_id":"tci2510c042714544","title":"TCI C0427 79-63-0 Lanosterol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0427 Lanosterol (CAS 79-63-0) is a triterpenoid sterol that occupies a central position in the eukaryotic sterol biosynthesis pathway. It serves as a substrate and reference compound in studies of sterol 14α-demethylase, the enzyme targeted by azole antifungal agents. Researchers also use it to examine membrane properties, mevalonate pathway intermediates, and lens protein aggregation. The powder should be kept tightly closed in a cool, dark, and dry place, and weighed with gloves and eye protection in a well-ventilated area.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eRisley (2002). Cholesterol Biosynthesis: Lanosterol to Cholesterol. \u003cem\u003eJournal of Chemical Education\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1021\/ed079p377\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1021\/ed079p377\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eShanmugam et al. (2015). Effect of lanosterol on human cataract nucleus. \u003cem\u003eIndian Journal of Ophthalmology\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.4103\/0301-4738.176040\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.4103\/0301-4738.176040\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eTuck et al. (1991). Lanosterol 14 alpha-demethylase (P45014DM): effects of P45014DM inhibitors on sterol biosynthesis downstream of lanosterol.. \u003cem\u003eJournal of Lipid Research\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/s0022-2275(20)41987-x\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/s0022-2275(20)41987-x\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085998207194,"sku":"TCI2510C042714544","price":3837000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0427.jpg?v=1768816243"},{"product_id":"tci2510c043414550","title":"TCI C0434 458-37-7 Curcumin (Natural)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCurcumin (Natural) TCI C0434, with CAS number 458-37-7, is a chemical compound widely used in scientific experiments, particularly in the fields of chemistry and biology. As a natural pigment derived from the root of the turmeric plant, it serves as a valuable dye in laboratory settings. This compound is commonly used to create colorimetric solutions for various analytical processes, including color tests, compound identification, and the study of chemical and biological properties. Its presence in pure form allows researchers to precisely control concentration levels and chemical reactions, making it an essential tool in experimental research.\u003c\/p\u003e\n\u003cp\u003eCurcumin is valued for its chemical stability under certain conditions, although it is highly sensitive to light and oxidation. These properties make it a preferred choice for applications where accurate and consistent results are crucial. Its natural origin also adds to its appeal, especially in studies focused on bioactive compounds. The compound’s antioxidant properties further enhance its utility in pharmacological and nutritional research, offering researchers a versatile material for a wide range of investigations.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, curcumin is frequently used in research related to the bioactivity of natural compounds. It plays a key role in studies examining anti-inflammatory and antioxidant effects, contributing to advancements in both scientific and applied research. Its availability and reliability make it a staple in many research environments, supporting the pursuit of knowledge in various scientific disciplines.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eColorimetric analysis is a common application where curcumin is used to detect and quantify specific compounds through color changes, making it ideal for qualitative and quantitative testing.\u003c\/li\u003e\n\u003cli\u003eBioactivity studies benefit from curcumin’s natural origin and antioxidant properties, enabling researchers to investigate its effects on cellular processes and biological systems.\u003c\/li\u003e\n\u003cli\u003eChemical identification processes rely on curcumin’s distinct color properties, allowing for the visualization and analysis of compounds in solution.\u003c\/li\u003e\n\u003cli\u003ePharmacological research utilizes curcumin to explore its potential therapeutic applications, particularly in inflammation and oxidative stress-related conditions.\u003c\/li\u003e\n\u003cli\u003eNutritional studies incorporate curcumin to assess its role in dietary supplements and its impact on human health, supporting research in food science and health sciences.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 458-37-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Stains and Dyes (for Research and Experimental Use) \u0026gt; Basic Dyes (for Research and Experimental Use)\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003eStorage note: Must be stored in a cool, dark place to prevent degradation due to light and oxidation\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCurcumin should be stored in a cool, dark environment to maintain its chemical integrity and prevent degradation caused by light exposure and oxidation. It is recommended to keep it in airtight containers to minimize contact with air and moisture. Due to its sensitivity, it is important to avoid prolonged exposure to heat and direct sunlight. In laboratory settings, curcumin should be handled with care to prevent contamination and ensure accurate experimental results. Proper labeling and storage conditions are essential for maintaining the quality and effectiveness of this compound in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085998436570,"sku":"TCI2510C043414550","price":607000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085998469338,"sku":"TCI2510C043414551","price":2550000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0434.jpg?v=1767095223"},{"product_id":"tci2510c061014819","title":"TCI C0610 910-31-6 Cholesteryl Chloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0610 Cholesteryl Chloride is a cholesterol derivative in which the 3-hydroxy group is replaced by chlorine, preserving the rigid chiral steroid framework. It is studied primarily as a cholesteric liquid crystal material, where helical molecular ordering produces selective reflection and optical rotation. Researchers commonly combine it with cholesteryl esters to build thermochromic mixtures and to investigate phase-transition behaviour. Supplied as a 25 g solid, it should be kept tightly closed in a cool, dry place away from light.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSharma et al. (2005). Theoretical mechanism of the formation of cholesteryl chloride from cholesterol and thionyl chloride. \u003cem\u003eJournal of Molecular Modeling\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1007\/s00894-004-0232-7\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1007\/s00894-004-0232-7\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eSayin et al. (2011). Magnetic properties of gamma irradiated single crystals of cholesteryl chloride: An EPR study. \u003cem\u003eRadiation Physics and Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.radphyschem.2011.06.002\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.radphyschem.2011.06.002\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086013182170,"sku":"TCI2510C061014819","price":2500000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0610.jpg?v=1768816286"},{"product_id":"tci2510c069514940","title":"TCI C0695 516-91-6 Cholesteryl Bromide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0695 Cholesteryl Bromide is a cholesterol derivative in which the hydroxyl group is replaced by a bromine atom. The bromide serves as a leaving group, making the compound a useful precursor for preparing a wide range of cholesteryl derivatives. Its rigid chiral steroid core also makes it relevant to cholesteric liquid crystal and steroid chemistry research. AMI Scientific offers this TCI solid in a research package size; handle it with gloves and eye protection in a well-ventilated area and store it cool, dry, and protected from light per the official label and SDS.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"10g","offer_id":48086021275866,"sku":"TCI2510C069514940","price":4342000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0695.jpg?v=1768816314"},{"product_id":"tci2510c075014998","title":"TCI C0750 474-25-9 Chenodeoxycholic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0750 Chenodeoxycholic Acid is a naturally occurring primary bile acid belonging to the steroid class of biochemicals. Its amphiphilic structure underpins micelle formation and makes it a valuable reference compound in lipid and bile acid research. Laboratories commonly use it in bile acid signaling studies, cholesterol metabolism research, and as a reference standard for chromatographic profiling. AMI Scientific supplies this TCI product in a 5 g pack size for research use only.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePiazza (2000). Competition in liver transport between chenodeoxycholic acid and ursodeoxycholic acid as a mechanism for ursodeoxycholic acid and its amidates' protection of liver damage induced by chenodeoxycholic acid. \u003cem\u003eDigestive and Liver Disease\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/s1590-8658(00)80025-0\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/s1590-8658(00)80025-0\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eBortolini et al. (1996). A New Non-enzymatic Route to Chenodeoxycholic Acid. \u003cem\u003eChemistry Letters\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1246\/cl.1996.335\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1246\/cl.1996.335\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eZhang et al. (2015). Development of an enzyme-linked immunosorbent assay for chenodeoxycholic acid using an anti-chenodeoxycholic acid monoclonal antibody. \u003cem\u003eAnalytical Methods\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1039\/c5ay00733j\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1039\/c5ay00733j\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48276744962266,"sku":"TCI2510C075014998","price":1187000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0750.jpg?v=1768816328"},{"product_id":"tci2510c079615063","title":"TCI C0796 87-44-5 beta-Caryophyllene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0796 beta-Caryophyllene (CAS 87-44-5) is a naturally occurring bicyclic sesquiterpene widely associated with clove and black pepper aroma profiles. Supplied by AMI Scientific in 25 mL, 100 mL, and 500 mL presentations, it serves as a dependable reference material for essential oil characterisation and phytochemical research. Its distinctive fused ring framework also makes it a useful starting point for the preparation of terpene derivatives. Please consult the official TCI Certificate of Analysis and Safety Data Sheet before use.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eJ Bell (2021). Beta-Caryophyllene, an Anti-Inflammatory Natural Compound, Improves Cognition in an Elderly Group who has Concerns about Memory. \u003cem\u003eMedical Journal of Clinical Trials \u0026amp; Case Studies\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.23880\/mjccs-16000300\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.23880\/mjccs-16000300\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eBOLAT et al. (2025). Mechanistic Insights into the Mitigating Role of Beta-Caryophyllene on Cadmium-Induced Liver Injury. \u003cem\u003eKafkas Universitesi Veteriner Fakultesi Dergisi\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.9775\/kvfd.2025.34135\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.9775\/kvfd.2025.34135\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eOppong‐Damoah et al. (2019). Caryophyllene Oxide is More Potent than Beta Caryophyllene in Attenuating the Abuse‐Related Effects of Ethanol. \u003cem\u003eThe FASEB Journal\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1096\/fasebj.2019.33.1_supplement.499.6\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1096\/fasebj.2019.33.1_supplement.499.6\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48086029402330,"sku":"TCI2510C079615063","price":733000.0,"currency_code":"IDR","in_stock":true},{"title":"100mL","offer_id":48086029435098,"sku":"TCI2510C079615064","price":1515000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48086029467866,"sku":"TCI2510C079615065","price":3560000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0796.jpg?v=1769144547"},{"product_id":"tci2510c094115277","title":"TCI C0941 637-07-0 Clofibrate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eClofibrate is the ethyl ester of 2-(4-chlorophenoxy)isobutyric acid and a classic member of the fibrate class of compounds. In research settings it is widely cited as a reference PPARα agonist and is used to study lipid metabolism, hepatic biochemistry, and related cellular responses. Its ester group is readily hydrolysed to the corresponding free acid, making it a useful substrate in esterase and prodrug conversion studies, as well as a reference standard in HPLC and LC-MS method development. TCI supplies this oily liquid in 25 g and 500 g packs for laboratory research use only; store tightly closed, cool, and protected from light.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003e\u0026amp;NA; (1991). Clofibrate. \u003cem\u003eReactions Weekly\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.2165\/00128415-199103490-00020\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.2165\/00128415-199103490-00020\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003e\u0026amp;NA; (1992). Clofibrate. \u003cem\u003eInpharma Weekly\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.2165\/00128413-199208510-00001\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.2165\/00128413-199208510-00001\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eNAKAMURA et al. (2001). Characterization of Clofibrate-induced Retrograde Golgi Membrane Movement to the Endoplasmic Reticulum: Clofibrate Distinguishes the Golgi from the Trans Golgi Network. \u003cem\u003eBioscience, Biotechnology, and Biochemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1271\/bbb.65.1812\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1271\/bbb.65.1812\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086039003354,"sku":"TCI2510C094115277","price":2121000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086039036122,"sku":"TCI2510C094115278","price":16833000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0941.jpg?v=1767096039"},{"product_id":"tci2510c109515503","title":"TCI C1095 298-46-4 Carbamazepin","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCarbamazepine is a chemical compound widely used in pharmacological and biochemical research. As a key pharmaceutical research reagent, it plays a crucial role in experimental studies related to neurological disorders and the pharmacological effects on the central nervous system. This compound is essential for understanding the mechanisms of drug action and developing new therapeutic approaches. Produced by TCI, Carbamazepine is a reliable reagent for laboratory experiments, offering consistent results and high performance in various research settings.\u003c\/p\u003e\n\u003cp\u003eCarbamazepine is valued for its chemical stability and availability in solid form, which simplifies handling and application in the laboratory. It dissolves well in organic solvents, making it suitable for a wide range of chemical reactions and isolation processes. These properties ensure its effectiveness in both qualitative and quantitative analyses. Its compatibility with various experimental protocols makes it a preferred choice for researchers seeking precision and reliability in their work.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Carbamazepine is commonly used in pharmaceutical and biomedical research. It is integral to drug development, efficacy testing, and the study of drug mechanisms. Its availability in the local market supports independent experimentation and research activities, enabling scientists to conduct studies without external dependencies. This reagent is a fundamental component in advancing scientific knowledge and innovation in the field of pharmacology.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePharmaceutical Research: Carbamazepine is used in drug development to study the pharmacological effects and mechanisms of action of new compounds.\u003c\/li\u003e\n\u003cli\u003eNeurological Studies: It is essential for investigating the impact of drugs on the central nervous system and treating neurological disorders.\u003c\/li\u003e\n\u003cli\u003eBiochemical Analysis: Its solubility in organic solvents makes it ideal for biochemical assays and compound synthesis.\u003c\/li\u003e\n\u003cli\u003eDrug Efficacy Testing: Carbamazepine is employed to evaluate the effectiveness of pharmaceutical formulations in controlled environments.\u003c\/li\u003e\n\u003cli\u003eTherapeutic Mechanism Studies: It aids in understanding how drugs interact with biological systems and influence physiological responses.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 298-46-4\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Pharmaceutical Research Reagents\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCarbamazepine should be stored in a cool, dry place away from direct light to maintain its chemical stability. It is recommended to use airtight containers to prevent moisture absorption and contamination. Due to its solid form, it is easy to handle and measure accurately in laboratory settings. Researchers should ensure proper ventilation when working with this compound to minimize exposure. Avoid contact with incompatible substances to maintain the integrity of the reagent. Regular inspection of storage conditions is advised to ensure optimal performance and safety in laboratory operations.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"10g","offer_id":48086048342234,"sku":"TCI2510C109515503","price":1642000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086048375002,"sku":"TCI2510C109515504","price":3231000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1095.jpg?v=1769144516"},{"product_id":"tci2510c122215687","title":"TCI C1222 1250-95-9 Cholesterol-5alpha,6alpha-epoxide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1222 Cholesterol-5alpha,6alpha-epoxide (CAS 1250-95-9) is an oxidized cholesterol derivative belonging to the oxysterol family, with a defined alpha configuration at the 5,6-epoxide. It serves as a valuable reference compound in cholesterol oxidation research, lipid analysis, and membrane biology studies. Its well-defined stereochemistry supports reliable identification and quantification by chromatographic and mass spectrometric methods. AMI Scientific supplies this TCI steroid reagent in a 1 g pack size, and cold, light-protected storage is recommended in line with the manufacturer's label.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086057353434,"sku":"TCI2510C122215687","price":5527000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1222.jpg?v=1768816457"},{"product_id":"tci2510c131715812","title":"TCI C1317 53-06-5 Cortisone","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1317 Cortisone is a classic glucocorticoid steroid widely used as a biochemical reagent and reference compound in life science research. It is closely linked to cortisol through 11β-hydroxysteroid dehydrogenase activity, making it a common substrate in steroid metabolism studies. Laboratories also employ it as an analytical standard for HPLC and LC-MS hormone profiling and as a starting material for steroid derivatisation. AMI Scientific supplies this TCI product in a 1 g pack for research use only, and it should be stored cool, dry, and protected from light.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eClinic for Ear, Nose and Throat Medicine, Bundeswehr Central Hospital, Germany et al. (2025). Intratympanic Cortisone Injection: An Evaluation of the Current Data Situation. \u003cem\u003eInternational Journal of Health Policy Planning\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.33140\/ijhpp.04.01.01\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.33140\/ijhpp.04.01.01\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eAlsop et al. (2016). The Lipid Bilayer Provides a Site for Cortisone Crystallization at High Cortisone Concentrations. \u003cem\u003eScientific Reports\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1038\/srep22425\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1038\/srep22425\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eNomura et al. (1997). Circadian rhythms in plasma cortisone and cortisol and the cortisone\/cortisol ratio. \u003cem\u003eClinica Chimica Acta\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/s0009-8981(97)00142-3\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/s0009-8981(97)00142-3\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086062825690,"sku":"TCI2510C131715812","price":2171000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1317.jpg?v=1767096731"},{"product_id":"tci2510c136615886","title":"TCI C1366 601-57-0 (+)-4-Cholesten-3-one","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1366 (+)-4-Cholesten-3-one (CAS 601-57-0) is a steroid reagent widely used in biochemical and lipid research. It is commonly encountered as the enzymatic oxidation product of cholesterol, which makes it a convenient reference material for cholesterol oxidase studies and chromatographic comparison. Researchers also apply it in sterol metabolism work, membrane biology, and as a starting scaffold for further steroid synthesis. AMI Scientific supplies this TCI-branded product in a 5 g pack for laboratories in Indonesia.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086065938650,"sku":"TCI2510C136615886","price":3005000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1366.jpg?v=1768816499"},{"product_id":"tci2510c140615944","title":"TCI C1406 2154-68-9 3-Carboxy-2,2,5,5-tetramethylpyrrolidine 1-Oxyl Free Radical","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e3-Carboxy-2,2,5,5-tetramethylpyrrolidine 1-Oxyl Free Radical, commonly known as 3-carboxy-PROXYL, is a nitroxide free radical compound that remains stable at room temperature. Unlike ordinary free radicals, which are extremely short-lived, the unpaired electron on the nitroxide group of this compound is shielded by four surrounding methyl groups, allowing the material to be stored and handled like any conventional laboratory chemical. In the laboratory it serves as a spin probe and spin label in electron spin resonance spectroscopy, as well as a reagent in radical chemistry studies and oxidative stress research.\u003c\/p\u003e\n\u003cp\u003eThe principal characteristic that makes this compound a preferred choice is its distinctive and easily recognisable electron spin resonance signal, which arises from the interaction between the unpaired electron and the nitrogen nucleus. This signal pattern is highly sensitive to the surrounding environment, so that changes in viscosity, polarity, oxygen content, or molecular motion can be read directly from the shape of the spectrum. The carboxyl group at position 3 adds two further advantages: it improves solubility in aqueous media and provides a chemical attachment point for covalently binding the probe to proteins, lipids, polymers, and other molecules of interest.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is typically used in university research groups, government research institutes, and industrial laboratories that operate electron spin resonance instrumentation or conduct work on radical chemistry. It is generally handled in small quantities for spectroscopic measurement, method development, and comparative studies, and is requested alongside other analytical-grade reagents by teams working on oxidative stress, materials characterisation, and biomolecular labelling.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eElectron spin resonance spectroscopy — the compound produces a characteristic, easily identified signal from the unpaired electron interacting with the nitrogen nucleus, making it a dependable reference probe for instrument work.\u003c\/li\u003e\n\u003cli\u003eSpin probe measurement of the local environment — because the signal pattern responds to viscosity, polarity, and molecular motion, changes in the surrounding medium can be read directly from the spectral shape.\u003c\/li\u003e\n\u003cli\u003eOxygen-sensitive measurements — the sensitivity of the resonance signal to oxygen content allows researchers to follow variations in oxygen levels within a sample system under study.\u003c\/li\u003e\n\u003cli\u003eSpin labelling of biomolecules and polymers — the carboxyl group at position 3 provides a chemical attachment point for covalently binding the probe to proteins, lipids, and polymers.\u003c\/li\u003e\n\u003cli\u003eRadical chemistry and oxidative stress research — as a stable nitroxide radical that can be stored and handled conventionally, it serves as a practical reagent for studies involving radical species.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eProduct code: C1406\u003c\/li\u003e\n\u003cli\u003eCAS number: 2154-68-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Synthetic Reagents \u0026gt; Radical Chemistry\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard catalogue pack sizes; please confirm the size required when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: store according to the conditions stated on the manufacturer's label and safety data sheet\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the compound in its original tightly closed container, kept in a cool, dry, and well-ventilated area away from direct sunlight and sources of heat or ignition. Follow the storage temperature stated on the manufacturer's label and safety data sheet. Use chemically compatible containers and keep them clearly labelled. Handle the material in a fume hood where appropriate, wearing a laboratory coat, safety glasses, and suitable gloves. Avoid contact with skin and eyes and avoid inhaling any dust. Transfer only the amount needed for the work at hand, close the container promptly after use, and consult the safety data sheet before handling and for disposal guidance.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086068166874,"sku":"TCI2510C140615944","price":5150000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1406.jpg?v=1769180347"},{"product_id":"tci2510c141215952","title":"TCI C1412 1448-36-8 Methyl Cholate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1412 Methyl Cholate (CAS 1448-36-8) is the methyl ester of cholic acid, a widely studied bile acid in biochemical and pharmaceutical research. Esterification improves solubility in organic solvents, making it a convenient starting material for steroid derivatisation. Its three hydroxyl groups and amphiphilic steroid backbone support applications in supramolecular chemistry and drug delivery design. AMI Scientific offers this TCI reagent in a 25 g pack suitable for laboratory-scale research.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eDavis et al. (2005). A Short Synthesis of Methyl 3α,7α,12α-Triaminocholanoate, the ‘Triaza-Analogue’ of Methyl Cholate. \u003cem\u003eSynlett\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1055\/s-2005-865221\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1055\/s-2005-865221\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eDavis et al. (1999). The \"Triamino-analogue\" of Methyl Cholate; A Practical, Large-Scale Synthesis. \u003cem\u003eSynlett\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1055\/s-1999-3114\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1055\/s-1999-3114\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eGoonewardena et al. (1991). Relative Size Effect on the Polymerization with Methyl Cholate Inclusion Compounds. \u003cem\u003ePolymer Journal\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1295\/polymj.23.1405\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1295\/polymj.23.1405\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086068429018,"sku":"TCI2510C141215952","price":5276000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1412.jpg?v=1768816514"},{"product_id":"tci2510c147816053","title":"TCI C1478 152-58-9 Cortexolone","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1478 Cortexolone (11-deoxycortisol, CAS 152-58-9) is a natural corticosteroid intermediate in the cortisol biosynthetic pathway. Life science laboratories use it as an analytical reference standard and as a substrate for studies of 11β-hydroxylase activity and adrenal function testing. Its 17α-hydroxy pregnane skeleton also serves as a starting point for the synthesis of steroid derivatives in medicinal chemistry. Supplied in a 1 g pack; follow the manufacturer's storage guidance, Certificate of Analysis, and Safety Data Sheet.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eShuvalova et al. (2003). Microbiological Transformation of Cortexolone into Hydrocortisone. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.200321167\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.200321167\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eReda F. Allam (2012). 11 β-Hydroxylation of cortexolone using immobilized Cunninghamella elegans protoplasts. \u003cem\u003eAFRICAN JOURNAL OF BIOTECHNOLOGY\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.5897\/ajb11.4135\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.5897\/ajb11.4135\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eParaszkiewicz et al. (1998). Cortexolone 11β-hydroxylation in protoplasts of Curvularia lunata. \u003cem\u003eJournal of Biotechnology\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/s0168-1656(98)00129-1\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/s0168-1656(98)00129-1\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086072492250,"sku":"TCI2510C147816053","price":3787000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1478.jpg?v=1768816539"},{"product_id":"tci2510c157816210","title":"TCI C1578 75621-03-3 3-[(3-Cholamidopropyl)dimethylammonio]-1-propanesulfonate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1578 CHAPS (CAS 75621-03-3) is a zwitterionic, bile-acid-derived surfactant widely used for the gentle solubilisation of hydrophobic components. Its steroid backbone paired with a dual-charged head group gives it strong solubilising power while remaining net-neutral in charge under common working conditions. Typical applications include membrane protein extraction, two-dimensional electrophoresis sample preparation, buffer formulation, and polymer interface studies. AMI Scientific offers this TCI reagent in convenient 1 g and 5 g packages; please refer to the official TCI documentation for full technical and safety information.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eTornel et al. (1991). Inhibition of cholinesterases by the zwitterionic detergent 3-[(3-cholamidopropyl)dimethylammonio]-1-propanesulfonate (CHAPS). \u003cem\u003eBioorganic Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/0045-2068(91)90038-q\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/0045-2068(91)90038-q\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eNomura (2001). Incomplete Dialysis of Protein Samples Containing 3-[(3-Cholamidopropyl)dimethylammonio]-1-propanesulfonate May Lead to Erroneous Estimation of Histidine Content on Amino Acid Analysis. \u003cem\u003eAnalytical Biochemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1006\/abio.2000.4971\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1006\/abio.2000.4971\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eShnigir et al. (2004). Transformation of Phospholipids by Cabbage Phospholipase D in Mixed Micelles Containing 3-[(3-Cholamidopropyl)dimethylammonio]-1-propanesulfonate. \u003cem\u003eApplied Biochemistry and Microbiology\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1023\/b:abim.0000025942.11918.39\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1023\/b:abim.0000025942.11918.39\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086078914778,"sku":"TCI2510C157816210","price":910000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086078947546,"sku":"TCI2510C157816211","price":2500000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1578.jpg?v=1769144457"},{"product_id":"tci2510c197116584","title":"TCI C1971 303-98-0 Coenzyme Q10","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCoenzyme Q10, also known as ubiquinol, is an essential organic compound that plays a crucial role in cellular energy metabolism. As a key component of mitochondria, it functions as an electron acceptor in the electron transport chain, facilitating the production of ATP, which is vital for various cellular activities. This compound is widely used in life science research, particularly in biochemical and physiological studies, where its role in energy production and antioxidant activity is of significant interest. Its presence in biological systems makes it a valuable tool for understanding metabolic processes and cellular function.\u003c\/p\u003e\n\u003cp\u003eCoenzyme Q10 is a stable compound that resists degradation under normal conditions, making it suitable for a wide range of laboratory experiments. Its lipid-soluble nature allows it to dissolve in organic solvents such as ethyl acetate and chloroform, which is advantageous for chemical reactions and molecular interactions. This property enhances its utility in biochemical assays and analytical techniques. Additionally, its chemical stability ensures consistent performance in research applications, contributing to reliable experimental outcomes.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Coenzyme Q10 is commonly used in both basic and applied research. It supports studies in biochemistry, pharmacology, and biotechnology, enabling researchers to explore cellular mechanisms and drug development. Its relevance in understanding metabolic pathways and antioxidant behavior makes it a key reagent in scientific investigations. The compound's versatility and reliability make it a preferred choice for researchers across various disciplines in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eEnergy metabolism research as it facilitates ATP production in mitochondrial processes.\u003c\/li\u003e\n\u003cli\u003eAntioxidant activity studies due to its ability to neutralize free radicals in cellular systems.\u003c\/li\u003e\n\u003cli\u003eBiochemical assays for analyzing electron transport chain efficiency in cellular respiration.\u003c\/li\u003e\n\u003cli\u003ePharmacological studies to evaluate its role in drug metabolism and therapeutic applications.\u003c\/li\u003e\n\u003cli\u003eMolecular interaction experiments because of its lipid-soluble nature and chemical stability.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 303-98-0\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Terpenes\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCoenzyme Q10 should be stored in a cool, dry place, away from direct light to maintain its chemical stability. It is recommended to use airtight containers to prevent moisture absorption and contamination. Since it is a lipid-soluble compound, it should be handled with care to avoid exposure to incompatible substances. Laboratory personnel should wear appropriate personal protective equipment when handling this material. Proper labeling of containers is essential for safety and traceability. Regular monitoring of storage conditions ensures the integrity of the compound for research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48086093496538,"sku":"TCI2510C197116584","price":910000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086093529306,"sku":"TCI2510C197116585","price":4342000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1971.jpg?v=1767097603"},{"product_id":"tci2510c230217033","title":"TCI C2302 458-37-7 Curcumin (Synthetic)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCurcumin (Synthetic) TCI C2302 is a chemical compound widely utilized in scientific research, particularly in the fields of biochemistry and pharmaceutical sciences. As a synthetic derivative of curcumin found naturally in turmeric, it serves as a key reagent in experimental studies aimed at understanding biological mechanisms and therapeutic potential. Its versatility makes it an essential component in laboratories conducting research on antioxidant, anti-inflammatory, and pharmacological properties of natural compounds. This compound is frequently employed in both qualitative and quantitative analyses, supporting a broad range of scientific investigations.\u003c\/p\u003e\n\u003cp\u003eCurcumin is prized for its chemical stability and solubility in organic solvents such as ethyl acetate and ethanol, which facilitates its use in various chemical reactions and analytical procedures. Its ability to react effectively with different substrates enhances its applicability in biological assays, making it a preferred choice for researchers seeking reliable and consistent results. Additionally, its high purity ensures accuracy in experiments that require precise measurements and reproducible outcomes. These properties contribute to its widespread use in both academic and industrial research settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, curcumin is commonly used in studies related to health, pharmacology, and nutrition. It is a favored material for investigating the bioavailability and efficacy of natural compounds, supporting research into potential therapeutic applications. Its availability and reliability make it a go-to option for scientists working on projects that require a stable and high-quality reagent. This compound plays a crucial role in advancing scientific knowledge and innovation in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBiochemical Research: Curcumin is used to study antioxidant and anti-inflammatory properties due to its chemical stability and reactivity.\u003c\/li\u003e\n\u003cli\u003ePharmacological Studies: It supports research into drug development by analyzing its pharmacological effects and biological interactions.\u003c\/li\u003e\n\u003cli\u003eNutritional Analysis: Curcumin is employed in studies assessing the bioavailability and health benefits of natural compounds in food.\u003c\/li\u003e\n\u003cli\u003eSynthetic Chemistry: Its solubility in organic solvents makes it ideal for chemical synthesis and compound modification.\u003c\/li\u003e\n\u003cli\u003eAnalytical Chemistry: It is used as a reagent in chromatographic and spectroscopic analyses due to its consistent chemical behavior.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS Number: 458-37-7\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Crude Medicine Ingredients for Research and Experimental Use\u003c\/li\u003e\n\u003cli\u003ePack Sizes: As per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical Form: Powder\u003c\/li\u003e\n\u003cli\u003eStorage Note: Store in a cool, dry place away from light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCurcumin should be stored in a cool, dry environment, away from direct sunlight and moisture to maintain its chemical stability. It is recommended to keep it in a tightly sealed container to prevent contamination and degradation. Due to its organic nature, it is best stored in glass or high-density polyethylene containers to ensure safety and purity. Avoid exposure to strong oxidizing agents or reactive substances to prevent unwanted chemical reactions. Proper labeling and storage conditions are essential to ensure its integrity and usability in laboratory settings. Always handle with care, using appropriate personal protective equipment when necessary.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086118367450,"sku":"TCI2510C230217033","price":1137000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086118400218,"sku":"TCI2510C230217034","price":3711000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2302.jpg?v=1767098099"},{"product_id":"tci2510c237017125","title":"TCI C2370 59729-32-7 Citalopram Hydrobromide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCitalopram Hydrobromide is a chemical compound widely used in pharmacological and biochemical research. It serves as a key reagent in laboratory settings, enabling scientists to study the effects of antidepressant drugs on the nervous system. This compound is particularly relevant in experimental studies aimed at understanding the mechanisms of action of selective serotonin reuptake inhibitors (SSRIs). Its role in pharmaceutical research makes it an essential tool for developing new therapeutic approaches and analyzing drug interactions.\u003c\/p\u003e\n\u003cp\u003eThe compound is known for its chemical stability and solubility in organic solvents such as ethylamine, which makes it highly versatile for various laboratory applications. Its predictable behavior under different experimental conditions ensures reliable results, making it a preferred choice for researchers. Additionally, its safety profile in experimental use allows for precise and repeatable studies, which is crucial in scientific research. The availability of this compound in multiple packaging sizes further enhances its usability across different experimental needs.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Citalopram Hydrobromide is commonly used in research related to anxiety and depression disorders. It plays a vital role in pharmacological studies, helping researchers explore the efficacy of antidepressant treatments. Its presence in local research facilities underscores its importance in advancing mental health studies and drug development efforts in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePharmacological research involving the study of antidepressant mechanisms in neurological models.\u003c\/li\u003e\n\u003cli\u003eBiochemical experiments to analyze drug interactions and receptor binding in cell cultures.\u003c\/li\u003e\n\u003cli\u003eDevelopment of therapeutic agents for mental health disorders through experimental formulation studies.\u003c\/li\u003e\n\u003cli\u003eAnalytical testing of drug efficacy and stability in controlled laboratory environments.\u003c\/li\u003e\n\u003cli\u003eInvestigation of the pharmacokinetic properties of antidepressants in preclinical studies.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 59729-32-7\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Pharmaceutical Research Reagents\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in multiple sizes to suit different experimental requirements\u003c\/li\u003e\n\u003cli\u003ePhysical form: Powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCitalopram Hydrobromide should be stored in a cool, dry place, away from direct light and moisture to maintain its chemical stability. It is recommended to use airtight containers to prevent exposure to humidity and contaminants. In laboratory settings, it should be handled with care to avoid inhalation or skin contact, following standard safety protocols. Proper labeling and storage conditions ensure the compound remains effective for experimental use. Regular monitoring of storage conditions is advised to maintain the integrity of the material during long-term use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086122758362,"sku":"TCI2510C237017125","price":2929000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086122791130,"sku":"TCI2510C237017126","price":10071000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2370.jpg?v=1768204654"},{"product_id":"tci2510c240817175","title":"TCI C2408 59865-13-3 Cyclosporin A","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCyclosporin A is a biochemical compound widely used in life sciences research. It serves as an active ingredient with potent immunosuppressive properties, making it essential for studies involving the immune system, inflammation, and autoimmune diseases. This compound plays a crucial role in various laboratory experiments, particularly in immunology and pharmacology. Its ability to modulate immune responses has made it a key tool in both basic and applied research settings. Cyclosporin A is also integral to drug development and therapeutic research, especially in the field of biomedicine.\u003c\/p\u003e\n\u003cp\u003eCyclosporin A is valued for its complex structure and stable chemical properties, which ensure consistent performance in laboratory applications. It exhibits good solubility in organic solvents, making it compatible with a wide range of experimental protocols. The compound’s non-toxic nature further enhances its safety profile, allowing researchers to use it without significant risk in controlled laboratory environments. These characteristics make Cyclosporin A a reliable and preferred choice for scientific investigations.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Cyclosporin A is commonly used in academic and research institutions. It is particularly relevant for studies on immunological mechanisms, drug development, and immunosuppressive therapies. Its versatility and reliability make it a valuable resource for researchers working in life sciences and biomedical fields. The compound is frequently utilized in both teaching and applied research settings across Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eImmunological research: Cyclosporin A is ideal for studying immune system modulation due to its strong immunosuppressive activity.\u003c\/li\u003e\n\u003cli\u003eAutoimmune disease studies: It is widely used to investigate the mechanisms of autoimmune disorders and potential therapeutic interventions.\u003c\/li\u003e\n\u003cli\u003ePharmacological research: The compound is essential for drug development and testing, especially in the field of immunosuppressive therapies.\u003c\/li\u003e\n\u003cli\u003eInflammatory response analysis: Cyclosporin A helps researchers understand the role of inflammation in various diseases and conditions.\u003c\/li\u003e\n\u003cli\u003eBiomedical applications: It is a key component in the development of new treatments and therapies for immune-related conditions.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 59865-13-3\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Antibiotics\u003c\/li\u003e\n\u003cli\u003ePack sizes: As per standard laboratory supply formats\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Requires proper storage conditions to maintain stability and potency\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCyclosporin A should be stored in a cool, dry place away from direct sunlight to maintain its chemical stability. It is recommended to keep the compound in airtight containers to prevent moisture absorption and contamination. Due to its non-toxic nature, it is generally safe to handle, but standard laboratory safety protocols should still be followed. Researchers should ensure proper ventilation when working with the compound and avoid prolonged exposure. The compound should be stored in a secure location to prevent accidental use or contamination. Regular monitoring of storage conditions is advised to ensure the integrity of the material throughout its shelf life.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48086125117658,"sku":"TCI2510C240817175","price":1237000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086125150426,"sku":"TCI2510C240817176","price":6285000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2408.jpg?v=1767098303"},{"product_id":"tci2510c248117258","title":"TCI C2481 69-09-0 Chlorpromazine Hydrochloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eChlorpromazine Hydrochloride is a chemical compound widely utilized in pharmacological and biochemical research. It serves as a key reagent in experimental studies, particularly in the investigation of central nervous system effects and the mechanisms of drug action. This compound is essential for understanding the pharmacological properties of antipsychotic and sedative drugs, making it a vital component in pharmaceutical research. Its versatility allows it to be employed in various experimental setups, supporting both qualitative and quantitative analysis in laboratory settings.\u003c\/p\u003e\n\u003cp\u003eThe compound is valued for its chemical stability and solubility in organic solvents, which enhances its utility in a range of biochemical reactions and analytical procedures. Its molecular structure enables it to interact effectively in diverse experimental conditions, making it a preferred choice for researchers. Additionally, its resistance to degradation ensures long-term storage and repeated use without compromising its effectiveness, which is crucial for maintaining the integrity of experimental results.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Chlorpromazine Hydrochloride is commonly used in scientific research conducted by universities and research institutions. It is frequently found in pharmacological experiments, particularly in studies related to drug mechanisms, central nervous system interactions, and biochemical pathways. Its presence in these laboratories underscores its importance in advancing scientific understanding and supporting experimental research.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePharmacological research for studying antipsychotic and sedative effects due to its known pharmacological activity.\u003c\/li\u003e\n\u003cli\u003eBiochemical experiments to analyze drug interactions and metabolic pathways in biological systems.\u003c\/li\u003e\n\u003cli\u003eDrug development studies to evaluate the efficacy and safety of new pharmaceutical compounds.\u003c\/li\u003e\n\u003cli\u003eNeuropharmacological investigations to explore the impact of drugs on the central nervous system.\u003c\/li\u003e\n\u003cli\u003eQuantitative analysis in laboratory settings for accurate measurement and comparison of experimental data.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 69-09-0\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Pharmaceutical Research Reagents\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory requirements\u003c\/li\u003e\n\u003cli\u003ePhysical form: Powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eChlorpromazine Hydrochloride should be stored in a cool, dry environment, away from direct sunlight and moisture to maintain its chemical stability. It is recommended to use airtight containers to prevent exposure to air and humidity, which could affect its integrity. Proper labeling of storage containers is essential to ensure safe handling and prevent cross-contamination. Laboratory personnel should wear appropriate personal protective equipment when handling the compound to minimize exposure. Regular monitoring of storage conditions is advised to ensure the compound remains suitable for use in experimental research.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086128459994,"sku":"TCI2510C248117258","price":934000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086128492762,"sku":"TCI2510C248117259","price":3508000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2481.jpg?v=1767098406"},{"product_id":"tci2510c260917430","title":"TCI C2609 485-35-8 (-)-Cytisine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(-)-Cytisine is a naturally occurring alkaloid widely used in scientific research, particularly in the fields of biochemistry and pharmacology. As a key reagent in laboratory settings, it plays a crucial role in both qualitative and quantitative analysis. Its chemical structure allows it to interact with various biological systems, making it an essential tool for studying the effects of alkaloids on neural pathways and metabolic processes. This compound is commonly utilized in experiments aimed at understanding the pharmacological properties of natural substances and their potential therapeutic applications.\u003c\/p\u003e\n\u003cp\u003eThe chemical stability of (-)-Cytisine under controlled conditions makes it a preferred choice for researchers seeking reliable and consistent results. Its ability to serve as a building block in the synthesis of other bioactive compounds further enhances its value in laboratory work. Additionally, its molecular complexity supports advanced research applications, such as drug development and the analysis of natural compounds. These properties ensure that (-)-Cytisine remains a versatile and essential component in many scientific investigations.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, (-)-Cytisine is frequently used by researchers in pharmacology, biochemistry, and health sciences. Its role in studying the pharmacological effects of natural compounds supports the development of new therapeutic agents. The compound's reliability and versatility make it a valuable resource for both academic and industrial research, contributing to the advancement of scientific knowledge in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eUsed in pharmacological research to study the effects of alkaloids on neural and metabolic systems.\u003c\/li\u003e\n\u003cli\u003eApplied in biochemical experiments to analyze the interaction of alkaloids with biological molecules.\u003c\/li\u003e\n\u003cli\u003eEmployed in the synthesis of bioactive compounds for drug development and therapeutic applications.\u003c\/li\u003e\n\u003cli\u003eUtilized in analytical chemistry for qualitative and quantitative analysis of alkaloid compounds.\u003c\/li\u003e\n\u003cli\u003eIncorporated in health sciences research to explore the potential of natural compounds in treating diseases.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 485-35-8\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Alkaloids\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Crystalline solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e(-)-Cytisine should be stored in a cool, dry place, away from direct light and sources of heat. It is recommended to use airtight containers to prevent moisture absorption and contamination. Due to its toxic and potentially irritating properties, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles. In laboratory settings, it is important to follow standard safety protocols to minimize exposure. Proper ventilation should be maintained when working with this compound to ensure a safe working environment. Always label containers clearly to avoid confusion and ensure safe handling.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48086135341274,"sku":"TCI2510C260917430","price":2273000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086135374042,"sku":"TCI2510C260917431","price":9817000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2609.jpg?v=1768816894"},{"product_id":"tci2510c261217435","title":"TCI C2612 25122-46-7 Clobetasol 17-Propionate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eClobetasol 17-Propionate is a pharmaceutical compound widely used in laboratory research for its potent anti-inflammatory and immunomodulatory properties. As a member of the glucocorticoid class, it plays a critical role in studying immune responses and inflammatory processes. This compound is essential for experimental work in pharmaceutical and biochemical research, where its ability to modulate immune activity is of great interest. Its use extends to the development of new therapeutic formulations and the investigation of skin diseases and allergic reactions.\u003c\/p\u003e\n\u003cp\u003eClobetasol 17-Propionate is valued for its chemical stability under controlled conditions and its strong biological activity. These characteristics make it a preferred choice for researchers aiming to conduct reliable and reproducible experiments. Its solid form facilitates easy handling, storage, and use in various laboratory settings. Additionally, its potency requires careful handling to prevent contamination or unintended reactions, ensuring the integrity of experimental results.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Clobetasol 17-Propionate is commonly used in pharmaceutical, medical, and biotechnology research. Scientists rely on this compound to develop new drug formulations, test therapeutic effectiveness, and explore the mechanisms behind inflammatory and immune-related diseases. Its presence in research labs supports advancements in both academic and applied scientific fields.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePharmaceutical Research: Used to develop new formulations and test the efficacy of anti-inflammatory and immunomodulatory drugs.\u003c\/li\u003e\n\u003cli\u003eToxicology Studies: Applied in toxicity testing to evaluate the safety and potential side effects of compounds in biological systems.\u003c\/li\u003e\n\u003cli\u003eSkin Disease Research: Utilized to study the mechanisms of skin inflammation and the effectiveness of topical treatments for dermatological conditions.\u003c\/li\u003e\n\u003cli\u003eAllergy Studies: Employed to investigate the immune responses and treatment options for allergic reactions and hypersensitivity.\u003c\/li\u003e\n\u003cli\u003eDrug Mechanism Analysis: Used to understand how corticosteroids interact with cellular pathways and influence immune responses in disease models.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 25122-46-7\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Pharmaceutical Research Reagents\u003c\/li\u003e\n\u003cli\u003ePack sizes: As available\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eClobetasol 17-Propionate should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical stability. It is recommended to use airtight containers to prevent contamination and exposure to air. Due to its potent biological activity, it should be handled with care using appropriate personal protective equipment. Laboratories should ensure that it is stored separately from incompatible substances to avoid any potential chemical interactions. Regular monitoring of storage conditions is essential to maintain the integrity and effectiveness of the compound for research purposes.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086137372890,"sku":"TCI2510C261217435","price":1515000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086137405658,"sku":"TCI2510C261217436","price":5300000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2612.jpg?v=1771058128"},{"product_id":"tci2510c294017841","title":"TCI C2940 96946-42-8 Cisatracurium Besylate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C2940 is Cisatracurium Besylate, a benzylisoquinolinium-class compound supplied as a pharmaceutical research reagent intended for experimental laboratory use. The molecule is one of the isomers within the atracurium group and is widely documented in the pharmacological literature as a non-depolarizing neuromuscular blocking agent. In a laboratory setting, this material serves as a reference substance and test compound for receptor pharmacology studies, analytical method development, and pharmaceutical chemistry research that requires an active compound with a clearly defined chemical identity and consistent quality from lot to lot.\u003c\/p\u003e\n\u003cp\u003eThe characteristics that make this material important to researchers are the distinctive nature of its stereochemistry and its degradation pathway. As a bis-quaternary ammonium compound, the molecule is strongly polar and carries a permanent charge, so its solubility behaviour and chromatographic separation differ markedly from those of ordinary neutral compounds. The atracurium family of compounds is also known to break down through Hofmann elimination, a process dependent on pH and temperature. That property makes the material a valuable subject for chemical stability studies, degradation kinetics work, and analytical method validation, where a well-characterised degradation route is an advantage rather than a limitation.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is typically used in university pharmacy and pharmaceutical chemistry departments, in research institutes, and in analytical laboratories developing or validating methods for compounds of this class. It is normally handled in small quantities as a reference and test material within controlled experimental work, supporting instructional research, method development, and stability investigations that require a compound whose chemical identity is unambiguous and reproducible across studies.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eReceptor pharmacology studies — the compound is well documented as a non-depolarizing neuromuscular blocking agent, making it a suitable test article for experimental investigations of receptor behaviour.\u003c\/li\u003e\n\u003cli\u003eAnalytical method development — its permanent charge and strongly polar character give distinctive chromatographic retention behaviour, providing a demanding and instructive test compound for separation method design.\u003c\/li\u003e\n\u003cli\u003eChemical stability studies — the known Hofmann elimination pathway, which depends on both pH and temperature, allows controlled examination of how storage and solution conditions affect compound integrity.\u003c\/li\u003e\n\u003cli\u003eDegradation kinetics research — the defined breakdown route of the atracurium group supports quantitative measurement of degradation rates under varied experimental temperature and pH conditions.\u003c\/li\u003e\n\u003cli\u003eAnalytical method validation — consistent chemical identity between lots makes the material appropriate as a reference substance when confirming the specificity and reliability of laboratory methods.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS Number: 96946-42-8\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Pharmaceutical Research Reagents (for Experimental Use)\u003c\/li\u003e\n\u003cli\u003eCompound class: Benzylisoquinolinium compound; bis-quaternary ammonium structure\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the pack sizes listed for this catalogue item\u003c\/li\u003e\n\u003cli\u003eStorage: store according to the conditions stated on the product label and accompanying documentation\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore this reagent in a cool place, protected from heat, light, and moisture, and follow the storage conditions indicated on the product label. Because the compound is susceptible to Hofmann elimination, which is influenced by pH and temperature, avoid unnecessary warming and prepare solutions only as required for immediate experimental use. Keep the material in tightly closed original containers, or in chemically compatible sealed glass containers when transferring, and label all vessels clearly. Handle only in a properly ventilated laboratory using appropriate personal protective equipment, including gloves, safety glasses, and a laboratory coat. This product is for experimental laboratory use and should be managed under normal institutional chemical handling and waste disposal procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48086203924698,"sku":"TCI2510C294017841","price":1818000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086203957466,"sku":"TCI2510C294017842","price":6310000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2940.jpg?v=1768204717"},{"product_id":"tci2510c294217843","title":"TCI C2942 427-51-0 Cyproterone Acetate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C2942 is Cyproterone Acetate, a synthetic steroid compound supplied as a pharmaceutical research reagent for experimental laboratory use. The molecule belongs to the modified pregnane steroid family and is widely documented in the endocrinology literature as both an antiandrogenic compound and a progestin. In a research setting, this material serves as a test compound for hormone receptor investigations, as an analytical reference substance during the development of steroid assay methods, and as a subject of medicinal chemistry studies examining the relationship between steroid structure and biological activity.\u003c\/p\u003e\n\u003cp\u003eThe properties that make this material valuable to researchers centre on its rigid, stereochemically defined four-ring steroid framework, complemented by an acetate ester group and a characteristic substitution pattern that distinguishes it from naturally occurring steroid hormones. Because the ring skeleton is conformationally rigid, the spatial orientation of its functional groups remains highly consistent from experiment to experiment, which makes the compound well suited to receptor binding studies and molecular modelling work. As a steroid, it is generally a crystalline solid with limited solubility in water but dissolves in organic solvents such as ethanol or dimethyl sulfoxide.\u003c\/p\u003e\n\u003cp\u003eWithin Indonesian laboratories, this reagent is typically handled in university pharmacy and pharmaceutical chemistry departments, biomedical and endocrinology research groups, and analytical method development units that work with steroid compounds. It is used strictly for experimental purposes, prepared as stock solutions in a suitable organic solvent before dilution into working systems, and applied in receptor studies, comparative analytical runs, and structure–activity investigations conducted under standard laboratory protocols.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eHormone receptor binding studies — the rigid steroid skeleton gives a consistent spatial arrangement of functional groups, making interaction data with receptor preparations reproducible between experimental runs.\u003c\/li\u003e\n\u003cli\u003eAnalytical reference material for steroid assay development — serves as a comparison substance when chromatographic or spectroscopic methods for steroid compounds are being established and validated in the laboratory.\u003c\/li\u003e\n\u003cli\u003eMedicinal chemistry structure–activity research — its distinctive substitution pattern relative to natural steroid hormones makes it a useful reference point for studying how structural modification affects biological activity.\u003c\/li\u003e\n\u003cli\u003eMolecular modelling and computational chemistry work — the stereochemically defined, conformationally rigid four-ring framework provides reliable geometry input for docking simulations and comparative structural analysis studies.\u003c\/li\u003e\n\u003cli\u003eEndocrinology teaching and experimental investigation — widely documented in the endocrinology literature as an antiandrogen and progestin, giving researchers ample published context to design and interpret experimental work.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 427-51-0\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Pharmaceutical Research Reagents (for Experimental Use)\u003c\/li\u003e\n\u003cli\u003eProduct code: C2942\u003c\/li\u003e\n\u003cli\u003ePhysical form: crystalline solid; limited solubility in water, soluble in organic solvents such as ethanol or dimethyl sulfoxide\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard research quantities — please refer to the catalogue listing for the packaging options offered\u003c\/li\u003e\n\u003cli\u003eStorage: keep in a tightly closed container in a cool, dry place away from light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the material in its original tightly closed container, in a cool, dry location protected from direct light and moisture, and follow the storage instructions printed on the product label and safety data sheet. Amber glass vials or the supplier's original packaging are appropriate containers; avoid transferring the solid into containers that do not seal properly. Handle the compound in a well-ventilated area or fume hood using gloves, safety glasses, and a laboratory coat, and avoid generating dust when weighing the crystalline solid. Stock solutions prepared in ethanol or dimethyl sulfoxide should be clearly labelled with the solvent, concentration, and preparation date, kept tightly capped, and handled only by trained personnel. This product is intended for experimental laboratory use only and is not for human or veterinary application; dispose of residues and contaminated consumables through the laboratory's established chemical waste procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48086204023002,"sku":"TCI2510C294217843","price":2399000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086204055770,"sku":"TCI2510C294217844","price":8355000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2942.jpg?v=1768204716"}],"url":"https:\/\/amiscientific.com\/en\/collections\/tci-l3-cell-signaling-and-neuroscience.oembed?page=32","provider":"AMI Scientific","version":"1.0","type":"link"}