{"title":"Co-Translational Modification","description":"\u003cp\u003e\u003cstrong\u003eCo-Translational Modification\u003c\/strong\u003e — menghimpun asam amino non-alami dan turunannya seperti lisin bertag TCO, azidonorleusin, serta tirosin termodifikasi yang dirancang untuk disisipkan ke dalam rantai protein selama proses translasi guna keperluan pelabelan maupun studi bioortogonal protein.\u003c\/p\u003e\u003cp\u003eAsam amino non-alami dalam kategori ini digunakan pada teknik penyisipan kode genetik yang diperluas (genetic code expansion) untuk memasukkan gugus reaktif seperti azida, alkuna, atau TCO ke posisi spesifik dalam rantai protein saat translasi. Peneliti bidang proteomik dan biologi kimia memanfaatkannya untuk pelabelan protein target secara selektif melalui reaksi klik atau ligasi bioortogonal tanpa mengganggu struktur protein asli.\u003c\/p\u003e\u003cp\u003eContoh produk dalam koleksi ini: \u003ca href=\"\/en\/products\/tci2510t412655870\"\u003eTCI T4126 1380349-88-1 N-(4E)-TCO-L-lysine\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b651113419\"\u003eTCI B6511 1262681-31-1 Biotin-PEG4-Alkyne\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510a35544387\"\u003eTCI A3554 1454334-76-9 L-Azidonorleucine Hydrochloride\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c377018859\"\u003eTCI C3770 7423-93-0 H-Tyr(3-Cl)-OH\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510a35504383\"\u003eTCI A3550 120042-14-0 L-Azidohomoalanine\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c395219068\"\u003eTCI C3952 939-69-5 6-Hydroxybenzo[d]thiazole-2-carbonitrile\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510a21712763\"\u003eTCI A2171 1946-82-3 Nalpha-Acetyl-L-lysine\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510d021319559\"\u003eTCI D0213 300-38-9 3,5-Dibromo-L-tyrosine\u003c\/a\u003e.\u003c\/p\u003e\u003cp\u003ePerhatikan kompatibilitas gugus reaktif (azida, alkuna, atau TCO) dengan sistem ekspresi protein yang dipakai, serta kemurnian dan bentuk garam asam amino sebelum digunakan dalam eksperimen. 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 Proteomics, sering dipakai bersamaan dalam satu alur kerja laboratorium:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-post-translational-modification\"\u003ePost-Translational Modification\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-protein-sample-preparation\"\u003eProtein Sample Preparation\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-protein-electrophoresis\"\u003eProtein Electrophoresis\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-protein-determination\"\u003eProtein Determination\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-protein-interaction\"\u003eProtein Interaction\u003c\/a\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eKembali ke \u003ca href=\"\/en\/collections\/tci-l3-proteomics\"\u003eProteomics\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":"tci2510b651113419","title":"TCI B6511 1262681-31-1 Biotin-PEG4-Alkyne","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6511 Biotin-PEG4-Alkyne (CAS 1262681-31-1) is a click chemistry reagent that combines a biotin tag, a hydrophilic PEG4 spacer, and a terminal alkyne. The alkyne reacts selectively with azide-modified biomolecules, while the biotin group enables streptavidin-based detection and pull-down. The PEG4 spacer improves solubility and provides distance between the tag and the labelled target. Supplied in a 50 mg pack, it is best aliquoted after dissolution and stored under the cold conditions stated on the manufacturer's label.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eLiu et al. (2023). Discovery of two biotin-PEG4‑diarylidenyl piperidone prodrugs as potent antitumor agents with good efficacy, limited toxicity, and low resistance. \u003cem\u003eBioorganic Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.bioorg.2022.106323\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.bioorg.2022.106323\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eWang et al. (2024). Design, docking optimization, and evaluation of biotin-PEG4-1,8-naphthalimide as a potent and safe antitumor agent with dual targeting of ferroptosis and DNA. \u003cem\u003eRSC Medicinal Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1039\/d4md00134f\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1039\/d4md00134f\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":"50mg","offer_id":48085944074458,"sku":"TCI2510B651113419","price":6915000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6511.jpg?v=1767093783"},{"product_id":"tci2510c377018859","title":"TCI C3770 7423-93-0 H-Tyr(3-Cl)-OH","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C3770 7423-93-0 H-Tyr(3-Cl)-OH is a chemical compound widely used in chemical biology and peptide chemistry. This compound is a derivative of tyrosine with a chlorine group at the third carbon position, making it a valuable reagent in the synthesis of complex peptides. Its unique structure allows it to participate in specific chemical reactions, which is essential for creating bioactive molecules with targeted functions. In laboratory settings, this compound plays a crucial role in the development of pharmaceuticals and biochemical analyses.\u003c\/p\u003e\n\u003cp\u003eThe compound's stability and reactivity make it a preferred choice for researchers. It can undergo various chemical reactions, including coupling and substitution, which are fundamental in peptide synthesis. Its predictable behavior and consistent performance ensure reliable results in experimental processes. These properties make it an ideal material for applications requiring precision and accuracy.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, TCI C3770 7423-93-0 H-Tyr(3-Cl)-OH is commonly used in biological chemistry research. It is particularly favored in academic institutions and research centers for its role in developing bioactive compounds. Its availability in various packaging options makes it suitable for both small-scale and large-scale experiments. This compound is essential for advancing scientific research in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePeptide Synthesis: This compound is ideal for synthesizing peptides with specific functional groups, enabling the creation of bioactive molecules with targeted biological activities.\u003c\/li\u003e\n\u003cli\u003eDrug Development: It is frequently used in pharmaceutical research to develop new drugs, as its structure allows for the incorporation of chlorine groups into therapeutic compounds.\u003c\/li\u003e\n\u003cli\u003eBiochemical Analysis: The compound is useful in biochemical assays where specific chemical modifications are required to study molecular interactions and biological functions.\u003c\/li\u003e\n\u003cli\u003eAcademic Research: It supports research in chemical biology, particularly in universities and research institutes where new compounds are being explored for their potential applications.\u003c\/li\u003e\n\u003cli\u003eStructural Chemistry Studies: Its unique chemical structure makes it valuable for studying the effects of substituents on molecular behavior and reactivity.\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: 7423-93-0\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various packaging options to suit different experimental needs\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or powder, depending on the specific product formulation\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in a sealed container to prevent exposure to moisture and air. Avoid storing it near heat sources or in areas with high humidity. When handling, ensure proper ventilation to minimize inhalation of any vapors. Use appropriate personal protective equipment such as gloves and safety goggles to prevent skin or eye contact. The compound is generally non-hazardous under normal conditions but should be treated with care to ensure safe laboratory practices.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086286401754,"sku":"TCI2510C377018859","price":2531000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086286434522,"sku":"TCI2510C377018860","price":10091000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3770.jpg?v=1769144252"},{"product_id":"tci2510c395219068","title":"TCI C3952 939-69-5 6-Hydroxybenzo[d]thiazole-2-carbonitrile","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e6-Hydroxybenzo[d]thiazole-2-carbonitrile is a chemical compound widely used in research applications within molecular biology and proteomics. This compound plays a crucial role in laboratory settings by supporting the synthesis of bioactive molecules and enabling the study of protein modifications. Its presence in various biochemical reactions makes it an essential tool for researchers aiming to develop new compounds or analyze biological processes. Its versatility allows it to be integrated into multiple experimental workflows, enhancing the accuracy and efficiency of scientific investigations.\u003c\/p\u003e\n\u003cp\u003eThe compound is valued for its complex chemical structure and its ability to form bonds with a wide range of organic molecules. These properties make it highly suitable for reactions requiring high specificity and selectivity. Additionally, its stability under certain conditions ensures that it remains effective throughout the research process. This stability simplifies storage and handling, making it a reliable choice for laboratory use. Its chemical reactivity also supports advanced analytical techniques, contributing to the advancement of scientific research in life sciences.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 6-Hydroxybenzo[d]thiazole-2-carbonitrile is frequently utilized by researchers in molecular biology, pharmacology, and health sciences. Its availability in the local market facilitates research activities without the need for imports. This accessibility supports the growth of scientific innovation and ensures that Indonesian researchers have the necessary tools to conduct high-quality experiments and contribute to global scientific knowledge.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMolecular Biology Research: This compound is used to study protein modifications and interactions, supporting the development of new therapeutic agents.\u003c\/li\u003e\n\u003cli\u003eProteomics Analysis: It aids in the synthesis of bioactive compounds, which are essential for analyzing complex protein structures and functions.\u003c\/li\u003e\n\u003cli\u003eDrug Development: Its chemical properties make it suitable for the creation of new pharmaceutical compounds with targeted biological activities.\u003c\/li\u003e\n\u003cli\u003eBiochemical Reactions: It is employed in reactions that require high specificity, enabling precise modifications of biomolecules.\u003c\/li\u003e\n\u003cli\u003eAnalytical Chemistry: Its stability and reactivity support advanced analytical techniques used in the characterization of organic compounds.\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: 939-69-5\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Molecular Biology \u0026gt; Proteomics\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory requirements\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\u003eThis compound should be stored in a cool, dry place, away from direct light and moisture to maintain its stability and effectiveness. It is recommended to use airtight containers to prevent exposure to air and contaminants. Due to its chemical reactivity, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. Proper ventilation is essential during handling to minimize inhalation risks. The compound should not be stored near incompatible materials to avoid potential chemical interactions. Regular monitoring of storage conditions is advised to ensure the compound remains in optimal condition for use in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086308585690,"sku":"TCI2510C395219068","price":3036000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3952.jpg?v=1768204809"},{"product_id":"tci2510d021319559","title":"TCI D0213 300-38-9 3,5-Dibromo-L-tyrosine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e3,5-Dibromo-L-tyrosine is a chemical compound widely used in laboratory experiments across chemistry and biochemistry. As a derivative of L-tyrosine, an essential amino acid found in proteins, it plays a vital role in the synthesis of complex molecules. This compound is particularly valuable in peptide chemistry and organic chemistry due to its unique chemical structure and reactivity. Its presence in laboratory settings allows researchers to explore molecular substitution reactions and the effects of bromine atoms on molecular stability.\u003c\/p\u003e\n\u003cp\u003eThe compound’s high reactivity and stability make it a preferred choice for various chemical processes. Its ability to participate in substitution, reduction, and oxidation reactions enhances its utility in synthetic pathways. Additionally, its solubility in organic solvents such as ethylamine and dimethyl sulfoxide facilitates its use in diverse experimental setups. The bromine substituents at positions 3 and 5 contribute to its reactivity, making it a key reagent in the development of bioactive compounds.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 3,5-Dibromo-L-tyrosine is commonly used in organic chemistry, biochemistry, and pharmacology research. It is frequently employed in the synthesis of complex molecules and in studies related to molecular structure and reactivity. Many research institutions and universities in Indonesia rely on this compound for advancing their scientific investigations in these fields.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis applications benefit from 3,5-Dibromo-L-tyrosine due to its reactivity and ability to participate in substitution reactions.\u003c\/li\u003e\n\u003cli\u003eBiochemical research utilizes this compound to study molecular structure and the effects of bromine substitution on amino acid derivatives.\u003c\/li\u003e\n\u003cli\u003ePeptide chemistry experiments often incorporate this material as a building block for the synthesis of complex peptides and bioactive compounds.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research leverages its unique properties for the development of new drug compounds and molecular modifications.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry uses this compound as a reference standard for spectroscopic and chromatographic analyses.\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: 300-38-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\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\u003e3,5-Dibromo-L-tyrosine should be stored in a cool, dry environment to maintain its chemical integrity. It is recommended to keep the compound in airtight containers to prevent moisture absorption and contamination. Due to its reactive nature, it should be handled with care using appropriate personal protective equipment. Avoid exposure to direct sunlight and ensure proper ventilation in the laboratory. The compound is generally stable under normal storage conditions but should be used promptly to maintain its effectiveness. Always follow standard laboratory safety protocols when working with this material.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086357704922,"sku":"TCI2510D021319559","price":1490000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086357737690,"sku":"TCI2510D021319560","price":4891000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D0213.jpg?v=1768204832"},{"product_id":"tci2510d061220138","title":"TCI D0612 18835-59-1 3,5-Diiodo-L-tyrosine Dihydrate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e3,5-Diiodo-L-tyrosine Dihydrate is a chemical compound widely used in biochemical experiments and scientific research. It is a dihydrate form of the amino acid L-tyrosine, with two iodine atoms incorporated at the third and fifth positions. This compound plays a crucial role in laboratory settings, particularly in the synthesis of various bioactive molecules and thyroid hormones. Its presence in research protocols highlights its importance in understanding metabolic pathways and biological functions.\u003c\/p\u003e\n\u003cp\u003eThe compound's chemical stability and reactivity make it a preferred choice for researchers. The iodine atoms contribute to its high reactivity, enabling it to participate in a variety of chemical reactions such as substitution, oxidation, and reduction. These properties allow it to be a versatile reagent in synthetic processes and analytical studies. Its ability to interact with a wide range of molecules further enhances its utility in diverse experimental applications.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 3,5-Diiodo-L-tyrosine Dihydrate is commonly used in biochemical research and pharmaceutical development. It is a key component in studies related to protein metabolism and biological activity. Its availability and high purity ensure consistent results in experiments requiring precision and reliability. Researchers rely on this compound for its predictable behavior and compatibility with various experimental conditions.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBiochemical Synthesis: This compound is ideal for synthesizing thyroid hormones and other bioactive molecules due to its iodine content and structural versatility.\u003c\/li\u003e\n\u003cli\u003eProtein Metabolism Studies: Its role in metabolic pathways makes it suitable for investigating how amino acids are processed and utilized in biological systems.\u003c\/li\u003e\n\u003cli\u003eHormone Research: The iodine atoms allow it to be a precursor in the production of thyroid hormones, making it valuable for endocrinology studies.\u003c\/li\u003e\n\u003cli\u003eAnalytical Chemistry: Its chemical stability and reactivity make it useful in various analytical techniques requiring precise reagent performance.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Development: It is used in the formulation of drugs and bioactive compounds due to its ability to interact with multiple molecular structures.\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: 18835-59-1\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Amino Acids\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Dihydrate 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\u003eThis compound should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to humidity and air, which may affect its stability. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to ensure that it is kept separate from incompatible substances to avoid any potential chemical interactions. Proper labeling and storage conditions are essential to ensure safety and maintain the compound's effectiveness in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086394699994,"sku":"TCI2510D061220138","price":985000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086394732762,"sku":"TCI2510D061220139","price":3458000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D0612.jpg?v=1767101633"},{"product_id":"tci2510h184734787","title":"TCI H1847 1694495-59-4 Alkyne Tyramide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eAlkyne Tyramide (CAS 1694495-59-4) is a functionalized tyramide reagent that carries a terminal alkyne group at the end of the molecule. The reagent is designed to combine two of the most powerful techniques in modern molecular biology: peroxidase-mediated tyramide signal amplification and azide-alkyne click chemistry. When the tyramide is activated by horseradish peroxidase in the presence of hydrogen peroxide, an extremely short-lived phenoxyl radical is generated that forms covalent bonds with electron-rich residues on nearby proteins, leaving an alkyne mark precisely at the target location.\u003c\/p\u003e\n\u003cp\u003eThe advantage that makes this reagent a preferred choice is the separation between the deposition step and the detection step. The alkyne group is small, biologically neutral, and causes almost no disturbance to the structure of the sample, yet it remains highly reactive toward azides through copper-catalyzed cycloaddition as well as copper-free variants. Researchers can therefore store a labeled sample and later choose whichever fluorescent dye, biotin, or mass probe suits the next experiment. The very narrow labeling radius, a consequence of the short radical lifetime, gives excellent spatial resolution.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent fits research groups at universities, hospital pathology units, and biotechnology institutes that already run peroxidase-based immunodetection and want to extend it toward proximity labeling and multiplexed imaging. It is typically handled in facilities equipped with fluorescence microscopy or flow cytometry, where the two-step workflow allows scarce clinical or field-collected specimens to be labeled once and then analyzed with several different reporters over time.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eTyramide signal amplification in immunohistochemistry, where the alkyne handle deposits at the antigen site and is later developed with an azide-linked reporter of choice.\u003c\/li\u003e\n\u003cli\u003eProximity labeling and protein interaction mapping, since the short radical lifetime confines the alkyne mark to molecules in the immediate neighborhood of the peroxidase.\u003c\/li\u003e\n\u003cli\u003eMultiplexed fluorescence imaging, because one deposition step can be revealed with different azide dyes, letting several targets be visualized in a single specimen.\u003c\/li\u003e\n\u003cli\u003eAffinity enrichment of labeled proteins, in which an azide-biotin probe is clicked onto the deposited alkyne so that tagged material can be pulled down for downstream analysis.\u003c\/li\u003e\n\u003cli\u003eIn situ hybridization signal enhancement, where the peroxidase-driven deposition intensifies weak probe signals while the bioorthogonal alkyne keeps detection chemistry flexible.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI, catalogue number H1847\u003c\/li\u003e\n\u003cli\u003eCAS number: 1694495-59-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Conjugation Chemistry \/ Click Chemistry\u003c\/li\u003e\n\u003cli\u003eProduct name: Alkyne Tyramide\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard research-scale packaging as listed by the manufacturer\u003c\/li\u003e\n\u003cli\u003eStorage: keep according to the manufacturer's stated conditions for this reagent\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the reagent in its original tightly closed container, protected from light and moisture, and follow the temperature conditions stated by the manufacturer on the product label. Amber glass vials or the supplied container are appropriate; avoid repeated opening at room temperature so that condensation does not reach the material. Prepare working solutions inside a fume hood or a suitable ventilated enclosure, and wear gloves, safety glasses, and a laboratory coat when weighing or dissolving the compound. Label all prepared solutions clearly, keep them separate from strong oxidizing agents, and dispose of residues and contaminated consumables through the laboratory's chemical waste procedure.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"50mg","offer_id":48087330259162,"sku":"TCI2510H184734787","price":3345000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H1847.jpg?v=1767118613"},{"product_id":"tci2510i007535037","title":"TCI I0075 70-78-0 3-Iodo-L-tyrosine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e3-Iodo-L-tyrosine is a chemical compound classified under the category of amino acids, commonly used in laboratory settings for biochemical and biological research. This compound plays a significant role in experiments related to protein metabolism and enzyme activity. As a derivative of the amino acid tyrosine, it features a unique chemical structure with iodine atoms that enhance its reactivity. This makes it a valuable tool for researchers seeking to study specific chemical reactions and molecular interactions. Its presence in various scientific studies highlights its importance in understanding biological processes at the molecular level.\u003c\/p\u003e\n\u003cp\u003eThe properties of 3-Iodo-L-tyrosine make it a preferred choice for laboratory use. It is chemically reactive, allowing it to participate in a wide range of chemical reactions. Its defined structure enables it to interact with various molecules, making it suitable for applications requiring precision and control. Additionally, its purity and stability under certain conditions ensure reliable results in experimental procedures. These characteristics make it an essential component in biochemistry and pharmacology research, where accuracy and reproducibility are critical.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 3-Iodo-L-tyrosine is widely used in biochemical and pharmacological studies. It is commonly applied in experiments that investigate the effects of compounds on enzyme activity or in the development of new pharmaceuticals. Researchers in Indonesia rely on this compound for its versatility and effectiveness in supporting scientific investigations. Its use underscores its importance in advancing research in life sciences and related fields.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBiochemical Research: 3-Iodo-L-tyrosine is used to study enzyme activity and protein metabolism due to its reactivity and defined structure.\u003c\/li\u003e\n\u003cli\u003ePharmacological Studies: This compound is applied in drug development to investigate how specific molecules interact with biological systems.\u003c\/li\u003e\n\u003cli\u003eChemical Synthesis: It serves as a building block in the synthesis of other compounds, allowing for the creation of complex molecules with precise modifications.\u003c\/li\u003e\n\u003cli\u003eMolecular Interaction Studies: Its ability to bind with various molecules makes it ideal for experiments examining molecular recognition and binding mechanisms.\u003c\/li\u003e\n\u003cli\u003eEnzyme Kinetics Analysis: The compound is used to assess how enzymes interact with substrates, providing insights into reaction mechanisms and efficiency.\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: 70-78-0\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Amino Acids\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid 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\u003e3-Iodo-L-tyrosine should be stored in a cool, dry place, away from light and moisture to maintain its stability and purity. It is recommended to use airtight containers to prevent exposure to air and humidity, which can affect its chemical integrity. Due to its reactivity, it should be handled in a well-ventilated area, and appropriate personal protective equipment should be worn when working with it. Care should be taken to avoid contamination and ensure safe handling procedures are followed in the laboratory environment. Proper storage and handling are essential to preserve the compound's effectiveness and ensure safe usage in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087352606938,"sku":"TCI2510I007535037","price":2110000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087352639706,"sku":"TCI2510I007535038","price":8096000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510I0075.jpg?v=1767118941"},{"product_id":"tci2510i121136615","title":"TCI I1211 20846-39-3 H-Phe(3-I)-OH","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI I1211 20846-39-3 H-Phe(3-I)-OH is a chemical compound widely used in laboratory settings, particularly in the fields of peptide chemistry and chemical biology. It is a derivative of phenylalanine with an iodine atom substituted at the third position, making it a valuable reagent for synthetic applications. This compound plays a crucial role in the development of peptides and organic molecules due to its specific chemical structure and reactivity. Its unique properties allow it to participate in complex chemical reactions, contributing to the synthesis of bioactive compounds and pharmaceuticals.\u003c\/p\u003e\n\u003cp\u003eThe compound is preferred for its stability under controlled conditions and its solubility in various organic solvents such as ethylamine and acetone. These characteristics ensure consistent performance in laboratory experiments, making it a reliable choice for researchers. Its high reactivity and structural specificity make it suitable for applications requiring precise chemical interactions. The compound's ability to maintain its integrity during synthesis processes further enhances its appeal in chemical research.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, TCI I1211 20846-39-3 H-Phe(3-I)-OH is commonly used in pharmacology, biochemical research, and material science studies. Its availability in the local market supports ongoing scientific investigations and facilitates the development of new compounds. Researchers in Indonesia rely on this compound for its predictable behavior and compatibility with various synthetic protocols. Its role in advancing scientific research underscores its importance in the laboratory environment.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePeptide Synthesis: This compound is ideal for synthesizing peptides due to its structural specificity and reactivity, allowing for precise molecular construction.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Reactions: Its solubility in organic solvents and chemical stability make it a preferred reagent in complex organic synthesis processes.\u003c\/li\u003e\n\u003cli\u003eBiochemical Research: It is used in studies involving enzyme interactions and molecular recognition due to its ability to mimic natural amino acid structures.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Development: The compound's role in creating bioactive molecules supports drug discovery and formulation research.\u003c\/li\u003e\n\u003cli\u003eMaterial Science Studies: Its chemical properties contribute to the development of new materials with specific functional characteristics.\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: 20846-39-3\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\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: Should be stored in a dry, cool place away from moisture and air exposure\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a dry, cool environment to maintain its chemical stability and prevent degradation. It is recommended to use airtight containers to minimize exposure to moisture and air, which can affect its integrity. Due to its sensitivity, it is important to handle it with care during preparation and use. Laboratory personnel should ensure proper ventilation when working with this compound to avoid any potential hazards. The compound should be kept away from incompatible materials to prevent unwanted chemical reactions. Regular monitoring of storage conditions is advised to ensure optimal performance and safety in the laboratory setting.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"250mg","offer_id":48087450648794,"sku":"TCI2510I121136615","price":6409000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510I1211.jpg?v=1768205658"},{"product_id":"tci2510i125036663","title":"TCI I1250 24250-85-9 H-Phe(4-I)-OH","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI I1250 24250-85-9 H-Phe(4-I)-OH is a chemical compound widely used in laboratory settings for chemical and biochemical experiments. This compound is essential in peptide chemistry and plays a critical role in the synthesis of complex molecules with specific biological activities. Its presence in research laboratories supports the development of new compounds and the study of molecular structures, making it a valuable tool for scientists working in various fields. The compound is particularly useful for its versatility in chemical reactions, allowing researchers to explore a wide range of synthetic pathways and molecular modifications.\u003c\/p\u003e\n\u003cp\u003eThe compound's chemical stability and reactivity make it a preferred choice for laboratory use. It can participate in various types of chemical reactions, including substitution and coupling reactions, which are fundamental in organic synthesis. Its specific molecular structure enables it to interact effectively with a variety of reagents and substrates, enhancing its applicability in different experimental setups. These properties make it a reliable and efficient material for researchers aiming to achieve precise and reproducible results in their experiments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, TCI I1250 24250-85-9 H-Phe(4-I)-OH is commonly used in pharmacology, biochemistry, and organic chemistry research. Local researchers rely on this compound for the development of new therapeutic compounds and for studying molecular interactions. Its availability and effectiveness have made it a popular choice among scientists working on drug discovery and molecular modification projects.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eUsed in peptide synthesis for creating modified amino acid sequences due to its structural compatibility with peptide chains.\u003c\/li\u003e\n\u003cli\u003eApplied in organic chemistry for synthesizing complex organic molecules through substitution and coupling reactions.\u003c\/li\u003e\n\u003cli\u003eUtilized in biochemistry research to study molecular interactions and biological activity of synthesized compounds.\u003c\/li\u003e\n\u003cli\u003eEmployed in pharmacology for developing new drug candidates with targeted biological effects.\u003c\/li\u003e\n\u003cli\u003eIntegrated into molecular modification studies to explore new chemical functionalities and molecular structures.\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: 24250-85-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\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\u003eThis compound should be stored in a cool, dry environment, away from direct light, to maintain its chemical stability and prevent degradation. It is recommended to use airtight containers to minimize exposure to moisture and contaminants. Proper labeling of containers is essential for safe handling and to avoid cross-contamination. Laboratory personnel should wear appropriate personal protective equipment, such as gloves and safety goggles, when handling the compound. It is important to ensure that the compound is stored in a well-ventilated area to prevent the accumulation of harmful vapors. Regular inspection of storage conditions and containers is advised to maintain the integrity of the material and ensure safe laboratory practices.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48087453204698,"sku":"TCI2510I125036663","price":2896000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510I1250.jpg?v=1769142788"},{"product_id":"tci2510m227640491","title":"TCI M2276 6230-11-1 O-Methyl-L-tyrosine","description":"\u003cp\u003e\u003cstrong\u003eO-Methyl-L-tyrosine\u003c\/strong\u003e (CAS 6230-11-1) is a high-quality chemical from TCI, supplied as \u003cstrong\u003eHPLC Grade\u003c\/strong\u003e.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eApplication:\u003c\/strong\u003e Synthesis reagent for a wide range of organic chemistry transformations in laboratory and industrial settings.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eSpecifications:\u003c\/strong\u003e\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003eMolecular formula: C10H13NO3\u003c\/li\u003e\n\u003cli\u003eCAS number: 6230-11-1\u003c\/li\u003e\n\u003cli\u003ePurity: \u0026gt;98.0%(HPLC)(T)\u003c\/li\u003e\n\u003cli\u003eTCI product code: M2276\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003e\u003cstrong\u003eSynonyms:\u003c\/strong\u003e 4-Methoxy-L-phenylalanine; 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