{"title":"Cell Biology","description":"\u003cp\u003e\u003cstrong\u003eCell Biology\u003c\/strong\u003e — menghimpun reagen riset biologi sel yang mencakup senyawa bioaktif kecil, pewarna sel dan jaringan, penanda untuk pencitraan, serta bahan uji terkait apoptosis, ferroptosis, paraptosis, metabolisme tulang, riset kanker, sistem imun, dan biologi sel punca. Reagen-reagen ini menjadi alat kerja standar dalam eksperimen biologi molekuler dan seluler di laboratorium riset.\u003c\/p\u003e\u003cp\u003eCell Biology dipakai peneliti untuk uji proliferasi dan viabilitas sel, fraksinasi sel, pewarnaan dan pencitraan sel\/jaringan, studi jalur pensinyalan sel dan neurosains, riset eksosom, mitokondria, metabolomik, nutrisi, obesitas dan diabetes, hingga model eksperimen kanker dan sistem imun\/inflamasi\/alergi. Senyawa bioaktif kecil dalam kategori ini berfungsi sebagai senyawa acuan untuk riset yang memodulasi jalur biologis tertentu pada model eksperimen in vitro.\u003c\/p\u003e\u003cp\u003eContoh produk dalam koleksi ini: \u003ca href=\"\/en\/products\/tci2510s032550160\"\u003eTCI S0325 112-63-0 Methyl Linoleate [Standard Material for GC]\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b552012169\"\u003eTCI B5520 714971-09-2 BMS-599626\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510s016350046\"\u003eTCI S0163 57-11-4 Stearic Acid\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b559212263\"\u003eTCI B5592 132-17-2 Benztropine Mesylate\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510o018044529\"\u003eTCI O0180 112-80-1 Oleic Acid\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b559312265\"\u003eTCI B5593 70363-83-6 Bis(1,3-dibutylbarbituric Acid) Trimethine Oxonol\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510l005036931\"\u003eTCI L0050 463-40-1 Linolenic Acid\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b570012413\"\u003eTCI B5700 10309-37-2 Bakuchiol\u003c\/a\u003e.\u003c\/p\u003e\u003cp\u003ePerhatikan kemurnian dan bentuk pelarutan (larutan stok, bubuk, atau terkonjugasi fluoresen) yang sesuai dengan protokol assay, serta spesifisitas target biologis yang dilaporkan pada tiap reagen. 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 Life Science, sering dipakai bersamaan dalam satu alur kerja laboratorium:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/biokimia-dan-reagen-hayati\"\u003eBiokimia \u0026amp; Reagen Hayati\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/riset-pengembangan-obat\"\u003eRiset Pengembangan Obat\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/biologi-sel\"\u003eBiologi Sel\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l2-glycoscience\"\u003eGlycoscience\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l2-molecular-biology\"\u003eMolecular Biology\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l2-microbiology\"\u003eMicrobiology\u003c\/a\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eKembali ke \u003ca href=\"\/en\/collections\/tci-l1-life-science\"\u003eLife Science\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":3740000.0,"currency_code":"IDR","in_stock":true},{"title":"50mg","offer_id":48085885059290,"sku":"TCI2510B552012170","price":12986000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5520.jpg?v=1771058686"},{"product_id":"tci2510b559312265","title":"TCI B5593 70363-83-6 Bis(1,3-dibutylbarbituric Acid) Trimethine Oxonol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBis(1,3-dibutylbarbituric Acid) Trimethine Oxonol (DiBAC4(3)) is an anionic voltage-sensitive fluorescent dye widely employed in cell biology research for monitoring membrane potential changes. It enters depolarized cells and binds to intracellular components, producing a measurable fluorescence signal ideal for flow cytometry and fluorescence microscopy applications. This compound is commonly applied in hematology and histology studies involving cell viability assessment, platelet activation, and cellular response analysis.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mg","offer_id":48085889712346,"sku":"TCI2510B559312265","price":2306000.0,"currency_code":"IDR","in_stock":true},{"title":"25mg","offer_id":48085889745114,"sku":"TCI2510B559312266","price":7562000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5593.jpg?v=1769180200"},{"product_id":"tci2510b570012413","title":"TCI B5700 10309-37-2 Bakuchiol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBakuchiol is a naturally occurring meroterpene phenol isolated from *Psoralea corylifolia* seeds, widely employed as a reference standard in biochemical and pharmacological research. It is commonly applied in studies investigating retinol-like gene expression modulation, collagen and elastin synthesis, as well as antioxidant and anti-inflammatory activities. This compound also serves as a key material in natural cosmeceutical formulation development and antimicrobial screening assays.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"250mg","offer_id":48085897871578,"sku":"TCI2510B570012413","price":6269000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5700.jpg?v=1768815865"},{"product_id":"tci2510b570712424","title":"TCI B5707 96187-53-0 Brequinar","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBrequinar (TCI B5707, CAS 96187-53-0) is a potent dihydroorotate dehydrogenase (DHODH) inhibitor used in pharmaceutical research to study de novo pyrimidine biosynthesis. It is widely applied in experimental models of oncology, immunology, and virology to investigate cell proliferation suppression via nucleotide metabolism blockade. This product is intended strictly for laboratory and experimental use only.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"20mg","offer_id":48085898494170,"sku":"TCI2510B570712424","price":3373000.0,"currency_code":"IDR","in_stock":true},{"title":"100mg","offer_id":48085898526938,"sku":"TCI2510B570712425","price":11805000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5707.jpg?v=1771058498"},{"product_id":"tci2510b573912468","title":"TCI B5739 1022-46-4 Bentranil","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBentranil (CAS 1022-46-4) is a high-purity benzoxazinone compound supplied by TCI, commonly utilized as a reference standard and research reagent in cell biology and nutrition science. It serves as a reliable analytical standard for chromatographic method development and instrument validation in life science laboratories. The compound is also employed as a model molecule in studies investigating cellular metabolic pathways and bioactivity screening, supporting both fundamental and applied nutrition research.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"250mg","offer_id":48085900230874,"sku":"TCI2510B573912468","price":3429000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48085900263642,"sku":"TCI2510B573912469","price":10259000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5739.jpg?v=1768204440"},{"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":5819000.0,"currency_code":"IDR","in_stock":true},{"title":"100mg","offer_id":48085901410522,"sku":"TCI2510B576212496","price":18184000.0,"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":"tci2510b588812660","title":"TCI B5888 866323-14-0 Belinostat","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBelinostat (TCI B5888) is a potent hydroxamate-based histone deacetylase (HDAC) inhibitor supplied as a high-purity pharmaceutical research reagent for experimental use. It is primarily employed in preclinical oncology studies to investigate epigenetic mechanisms, gene expression modulation, and apoptosis induction in various cancer cell lines. This product serves as a valuable tool in HDAC inhibitor screening, drug resistance research, and combination therapy development.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mg","offer_id":48085908521178,"sku":"TCI2510B588812660","price":2447000.0,"currency_code":"IDR","in_stock":true},{"title":"100mg","offer_id":48085908553946,"sku":"TCI2510B588812661","price":8011000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5888_d63ea2ae-929a-4256-92e9-e030d244bc08.jpg?v=1767863756"},{"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":5341000.0,"currency_code":"IDR","in_stock":true},{"title":"25mg","offer_id":48085908947162,"sku":"TCI2510B589812670","price":17426000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5898.jpg?v=1768815920"},{"product_id":"tci2510b595212731","title":"TCI B5952 69327-76-0 Buprofezin","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B5952 Buprofezin (CAS 69327-76-0) is a high-purity chitin synthesis inhibitor widely utilized in cell biology and nutrition research laboratories for studying insect growth regulation and molting mechanisms. This compound serves as an essential reference standard for analytical testing, enzyme activity assays, and insect cell culture studies investigating the interaction between nutrition and developmental pathways. Available in 5g and 25g packaging from TCI, it is a reliable reagent for toxicology research and chitin biosynthesis pathway analysis in invertebrate model organisms.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48085911371994,"sku":"TCI2510B595212731","price":2868000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085911404762,"sku":"TCI2510B595212732","price":9950000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5952.jpg?v=1768204462"},{"product_id":"tci2510b597112753","title":"TCI B5971 120638-55-3 Bromfenac Sodium Sesquihydrate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBromfenac Sodium Sesquihydrate is a potent COX-2 inhibitor widely utilized in biochemical and pharmacological research. It serves as a selective non-steroidal anti-inflammatory agent for studying arachidonic acid metabolism and prostaglandin biosynthesis pathways. This compound is commonly applied in enzyme inhibition assays, COX-2 expression studies, and as a reference standard in ophthalmic formulation development.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085912518874,"sku":"TCI2510B597112753","price":4105000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5971.jpg?v=1771057971"},{"product_id":"tci2510b605512859","title":"TCI B6055 182498-32-4 SB 225002","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6055 (SB 225002, CAS 182498-32-4) is a potent and selective non-peptide antagonist of the CXCR2 interleukin-8 (IL-8) receptor, widely utilized in cancer research and cell biology studies. This compound is commonly applied in investigations of tumor metastasis, angiogenesis, and inflammatory signaling pathways associated with oncogenesis. Available in 10 mg and 50 mg packaging options under the TCI brand, it is a reliable reagent for laboratories conducting advanced biomedical and pharmacological research.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"10mg","offer_id":48085917040858,"sku":"TCI2510B605512859","price":4189000.0,"currency_code":"IDR","in_stock":true},{"title":"50mg","offer_id":48085917073626,"sku":"TCI2510B605512860","price":13857000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6055.jpg?v=1768815963"},{"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":2755000.0,"currency_code":"IDR","in_stock":true},{"title":"25mg","offer_id":48085917171930,"sku":"TCI2510B605612862","price":9838000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6056.jpg?v=1768815966"},{"product_id":"tci2510b606012867","title":"TCI B6060 217645-70-0 BX 471","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBX 471 (CAS 217645-70-0) is a selective CCR1 antagonist widely utilized in cell biology and immunology research to investigate chemokine signaling pathways and leukocyte migration. This TCI product is suitable for in vitro studies involving receptor binding assays, pharmacological screening, and mechanistic exploration of inflammatory and autoimmune disease models. The compound is offered in 5 mg and 25 mg packaging options with high purity suitable for reproducible experimental workflows.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mg","offer_id":48085917335770,"sku":"TCI2510B606012867","price":6100000.0,"currency_code":"IDR","in_stock":true},{"title":"25mg","offer_id":48085917368538,"sku":"TCI2510B606012868","price":21613000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6060.jpg?v=1768815965"},{"product_id":"tci2510b608512896","title":"TCI B6085 4481-62-3 Betulonic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBetulonic Acid (CAS 4481-62-3) is a pentacyclic triterpenoid compound supplied by TCI, primarily utilized as a reference reagent in pharmaceutical and life science research. It is widely employed in experimental studies involving anti-inflammatory activity, cytotoxicity assays against cancer cell lines, and antiviral potential evaluation. This product is intended exclusively for laboratory research purposes and serves as a reliable standard for chromatographic analysis and synthetic derivatization of betulinic acid analogs.\u003c\/p\u003e\n\u003cp\u003e---\u003c\/p\u003e","brand":"TCI","offers":[{"title":"50mg","offer_id":48085918580954,"sku":"TCI2510B608512896","price":5847000.0,"currency_code":"IDR","in_stock":true},{"title":"250mg","offer_id":48085918613722,"sku":"TCI2510B608512897","price":18635000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6085.jpg?v=1768204482"},{"product_id":"tci2510b612312939","title":"TCI B6123 2156642-70-3 BIP","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6123 (CAS 2156642-70-3) is a high-purity BIP (dipyrromethene boron complex) dye specifically developed for photonic materials research. This compound belongs to the dipyrromethene dye family, which is widely recognized for its excellent photostability and high fluorescence quantum yield, making it suitable for applications such as fluorescent probes in bioimaging, active layers in organic light-emitting diodes (OLEDs), and organic laser dyes. It is also utilized in the development of optical sensors and organic-based solar energy conversion systems.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mg","offer_id":48085920907482,"sku":"TCI2510B612312939","price":2643000.0,"currency_code":"IDR","in_stock":true},{"title":"25mg","offer_id":48085920940250,"sku":"TCI2510B612312940","price":9219000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6123.jpg?v=1768815985"},{"product_id":"tci2510b618613014","title":"TCI B6186 7287-19-6 Prometryn","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003ePrometryn is a triazine-class herbicide compound commonly used as a reference standard in pesticide residue analysis and environmental monitoring studies. It acts as a photosystem II inhibitor, making it a valuable tool for plant physiology research and herbicide resistance studies. This high-purity TCI product is suitable for chromatographic applications and quantitative analysis across academic and testing laboratories.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48085923889370,"sku":"TCI2510B618613014","price":2334000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085923922138,"sku":"TCI2510B618613015","price":8404000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6186.jpg?v=1768204489"},{"product_id":"tci2510b623613067","title":"TCI B6236 23491-45-4 Bisbenzimide H 33258 (0.2mL*5) (1mg\/mL in Water) [for Cell Staining]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBisbenzimide H 33258 (Hoechst 33258) is a fluorescent DNA-binding dye supplied as a ready-to-use solution at 1 mg\/mL in water, packaged in five vials of 0.2 mL each. This product is widely used for nuclear staining in fluorescence microscopy and flow cytometry, as it readily permeates both live and fixed cell membranes. It is also commonly applied in cell cycle analysis, apoptosis detection, DNA quantification assays, and various fluorescence-based biochemical research.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1set","offer_id":48085925855450,"sku":"TCI2510B623613067","price":1097000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6236.jpg?v=1768816010"},{"product_id":"tci2510b629313131","title":"TCI B6293 82657-04-3 Bifenthrin","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBifenthrin TCI B6293 is a high-purity synthetic pyrethroid reference standard for analytical and life science research. It is commonly applied in cell biology and nutrition studies to investigate xenobiotic effects on metabolic pathways, oxidative stress responses, and cellular biotransformation mechanisms. This product also serves as a reliable standard for pesticide residue analysis in food safety and environmental toxicology research.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"250mg","offer_id":48085929099482,"sku":"TCI2510B629313131","price":2559000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48085929132250,"sku":"TCI2510B629313132","price":8966000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6293.jpg?v=1769180263"},{"product_id":"tci2510b634113198","title":"TCI B6341 149877-41-8 Bifenazate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBifenazate (CAS 149877-41-8) is a carbazate-class acaricide widely used as a research and reference material in pesticide residue analysis and crop protection studies. Laboratories rely on it as a comparison standard for LC-MS\/MS and GC-MS methods, for method validation and recovery testing, and for research into mite resistance mechanisms linked to mitochondrial electron transport. TCI product B6341 is supplied in a 1 g pack and is intended for research and analytical use rather than as a ready-to-use agricultural product. Handle it in a fume hood with appropriate personal protective equipment, prevent release into waterways, and follow the manufacturer's Safety Data Sheet.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eChee (2006). Efficient Synthesis of Bifenazate.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.200646128\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.200646128\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eWang et al. (2023). Ferric chloride assisted QuEChERS method for separate detection of bifenazate and bifenazate-diazene in citrus fruits and its field validation. \u003cem\u003eFood Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.foodchem.2023.136149\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.foodchem.2023.136149\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eEuropean Food Safety Authority (2012). Modification of the existing MRLs for bifenazate in currants (red, black and white), blackberries and raspberries. \u003cem\u003eEFSA Journal\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.2903\/j.efsa.2012.2577\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.2903\/j.efsa.2012.2577\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":48085931786458,"sku":"TCI2510B634113198","price":7674000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6341.jpg?v=1768204498"},{"product_id":"tci2510b644313334","title":"TCI B6443 113558-15-9 Baohuoside I","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6443 Baohuoside I (CAS 113558-15-9) is a naturally derived prenylated flavonoid glycoside supplied strictly for research and experimental use. It is widely used as a reference compound in phytochemical profiling and in HPLC or LC-MS analysis of plant extracts. The 25 mg pack size suits analytical method development and small-scale biological studies. Store the vial tightly closed under cold, dry, light-protected conditions and allow it to reach room temperature before opening to prevent condensation.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eZhang et al. (2019). Effect of 2″-O-Rhamnosyl Icariside II, Baohuoside I and Baohuoside II in Herba Epimedii on Cytotoxicity Indices in HL-7702 and HepG2 Cells. \u003cem\u003eMolecules\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.3390\/molecules24071263\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.3390\/molecules24071263\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eMa et al. (2005). Baohuoside-1 inhibits activated T cell proliferation at G1–S phase transition. \u003cem\u003eTransplant Immunology\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.trim.2005.05.002\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.trim.2005.05.002\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eLin et al. (2026). Baohuoside I Combated Cryptocaryon irritans via Dual Targeting of Parasite Apoptosis and Host Defense Enhancement. \u003cem\u003eAntioxidants\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.3390\/antiox15030396\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.3390\/antiox15030396\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":48085940502746,"sku":"TCI2510B644313334","price":8180000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6443.jpg?v=1767093684"},{"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":1941000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085942927578,"sku":"TCI2510B648513388","price":6578000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6485.jpg?v=1768204505"},{"product_id":"tci2510b649213395","title":"TCI B6492 94-80-4 Butyl 2-(2,4-Dichlorophenoxy)acetate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6492, Butyl 2-(2,4-Dichlorophenoxy)acetate (CAS 94-80-4), is the butyl ester of the phenoxy compound 2,4-D, a long-studied synthetic auxin analogue. Its greater lipophilicity relative to the free acid makes it valuable for plant physiology research, tissue culture studies, and investigations of environmental hydrolysis pathways. It is also widely used as a reference material in pesticide residue analysis by GC-MS and LC-MS\/MS in food, water, and soil matrices. AMI Scientific offers this TCI product in a 1 g pack for research, testing, and analytical use only, and users should follow local regulations and hazardous waste procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085943189722,"sku":"TCI2510B649213395","price":3149000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6492.jpg?v=1768204510"},{"product_id":"tci2510b649313396","title":"TCI B6493 52869-18-8 2-Benzamido-9,10-anthraquinone","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6493, 2-Benzamido-9,10-anthraquinone (CAS 52869-18-8), is a substituted anthraquinone bearing a benzamide group at the 2-position. The conjugated tricyclic anthraquinone scaffold is a classic motif in medicinal chemistry and dye chemistry, while the aromatic amide adds hydrogen-bonding capability and modifies solubility. Supplied as a 10 mg screening-scale pack, it suits small-scale bioactivity screening, structure–activity relationship studies, and photophysical characterisation by UV-Vis or fluorescence. AMI Scientific recommends careful analytical weighing, protection from light, and storage according to the manufacturer's label and safety data sheet.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"10mg","offer_id":48085943222490,"sku":"TCI2510B649313396","price":5116000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6493.jpg?v=1768816065"},{"product_id":"tci2510b650213405","title":"TCI B6502 321674-73-1 BIBR 1532","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6502 BIBR 1532 (CAS 321674-73-1) is a small-molecule research compound widely used as a telomerase inhibitor in cancer biology studies. Researchers apply it in cell culture experiments to probe telomere maintenance, replicative capacity, and tumour cell proliferation. The 25 mg research pack size is convenient for preparing stock solutions and running repeated assays with consistent material. Please handle the compound with standard laboratory protective equipment and follow the storage guidance stated on the manufacturer's label and safety documentation.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eRomaniuk-Drapała et al. (2025). Telomerase inhibitors TMPyP4 and BIBR 1532 show synergistic antitumor activity in combination with chemotherapeutic drugs. \u003cem\u003eScientific Reports\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1038\/s41598-025-13496-0\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1038\/s41598-025-13496-0\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eBarma et al. (2003). Inhibition of telomerase by BIBR 1532 and related analogues. \u003cem\u003eBioorganic \u0026amp; Medicinal Chemistry Letters\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/s0960-894x(03)00101-x\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/s0960-894x(03)00101-x\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eHilal et al. (2011). Caloric Restriction Decreases Telomerase Activity and Enhances BIBR 1532 Inhibition Response on MDA‐MB 231 Cell Line. \u003cem\u003eThe FASEB Journal\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1096\/fasebj.25.1_supplement.915.10\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1096\/fasebj.25.1_supplement.915.10\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":48085943550170,"sku":"TCI2510B650213405","price":3852000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6502.jpg?v=1769144623"},{"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":6156000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6544.jpg?v=1768204511"},{"product_id":"tci2510b654813475","title":"TCI B6548 33171-05-0 Bisdemethoxycurcumin","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBisdemethoxycurcumin (CAS 33171-05-0) is one of the three principal curcuminoids found in turmeric rhizome, differing from curcumin by the absence of methoxy groups on both aromatic rings. It is commonly used as a reference compound for curcuminoid profiling by HPLC or TLC, and for in vitro bioactivity studies where a single, defined curcuminoid is preferred over a crude extract. Curcuminoids are light sensitive and degrade under alkaline conditions, so the material should be stored cool, dry, and protected from light, with working solutions prepared fresh. AMI Scientific supplies it in a 1 g pack size for research and experimental use.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMohammadi et al. (2018). Inhibition of amyloid fibrillation of lysozyme by bisdemethoxycurcumin and diacetylbisdemethoxycurcumin. \u003cem\u003eBiophysical Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.bpc.2018.02.005\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.bpc.2018.02.005\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eLappichetpaiboon (2025). Anticandidal effects of bisdemethoxycurcumin \u0026amp; melatonin with dual light emitting diode in photodynamic therapy. \u003cem\u003ePhotodiagnosis and Photodynamic Therapy\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.pdpdt.2025.104797\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.pdpdt.2025.104797\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eJayaprakasha et al. (2006). Antioxidant activities of curcumin, demethoxycurcumin and bisdemethoxycurcumin. \u003cem\u003eFood Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.foodchem.2005.06.037\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.foodchem.2005.06.037\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":48085946630362,"sku":"TCI2510B654813475","price":3289000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6548.jpg?v=1767093878"},{"product_id":"tci2510b659413540","title":"TCI B6594 210302-17-3 BAM 15","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBAM 15 (TCI B6594, CAS 210302-17-3) is a mitochondrial protonophore widely used as an uncoupler in cell biology research. It dissipates the inner mitochondrial membrane potential and uncouples respiration from ATP synthesis, driving oxygen consumption toward maximal rates. Researchers value it because its action is directed at mitochondria with comparatively limited effect on plasma membrane potential, simplifying bioenergetic experiments. Supplied in a 25 mg pack for research use only, it is not intended for diagnostic or therapeutic applications.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eDopp (2013). BAM 150. \u003cem\u003eEducational Media Reviews Online\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.59236\/emro.v15i12a5545\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.59236\/emro.v15i12a5545\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003enejadaria et al. (2020). Prevalence of Glucose-6-Phosphate Dehydrogenase Deficiency in Neonates Hospitalized in Pasteur Hospital of Bam, Iran. \u003cem\u003eMedical Laboratory Journal\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.29252\/mlj.14.2.9\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.29252\/mlj.14.2.9\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eAsma et al. (2019). The Role of Social Capital on the Health Promotion Behaviors in Women Teachers at Bam Girls’ Schools. \u003cem\u003eJournal of Medicine and Life\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.25122\/jml-2019-0066\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.25122\/jml-2019-0066\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":48085949251802,"sku":"TCI2510B659413540","price":9726000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6594.jpg?v=1767093984"},{"product_id":"tci2510b666113624","title":"TCI B6661 301836-41-9 SB 431542 [Optimized for Cell Culture]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6661 is SB 431542 [Optimized for Cell Culture] (CAS 301836-41-9), a small molecule inhibitor of the TGF-β type I receptor ALK5, prepared with cell culture applications in mind. Because TGF-β signaling governs differentiation, proliferation, and epithelial–mesenchymal transition, this inhibitor is a common medium component in stem cell maintenance and organoid workflows. Researchers also use it in directed differentiation protocols and in vitro fibrosis models where controlled pathway suppression is required. AMI Scientific supplies this TCI product in a 5 mg pack size, convenient for preparing stock solutions for routine culture work.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mg","offer_id":48085952594138,"sku":"TCI2510B666113624","price":4470000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6661.jpg?v=1768204518"},{"product_id":"tci2510b672713654","title":"TCI B6727 30484-77-6 Flunarizine Dihydrochloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6727 Flunarizine Dihydrochloride (CAS 30484-77-6) is a diphenylpiperazine-class calcium channel blocker supplied as a pharmaceutical research reagent for experimental use. Researchers apply it as a pharmacological tool to probe calcium entry and related signalling pathways in cell and tissue models. The dihydrochloride salt form simplifies handling and stock solution preparation compared with the free base. AMI Scientific supplies the 25 g size, and the material is intended strictly for laboratory research rather than human, clinical, or therapeutic use.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAMJ et al. (2017). Flunarizine Dihydrochloride Nanoemulsion for Migraine Nasal Drug Delivery: Fabrication, Characterization and In Vitro Study. \u003cem\u003eDrug Delivery Letters\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.2174\/2210303106666160930113725\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.2174\/2210303106666160930113725\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eYelli et al. (2022). Development and validation of dissolution testing of Flunarizine dihydrochloride in tablet dosage form. \u003cem\u003ePharmacy Education\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.46542\/pe.2022.222.132137\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.46542\/pe.2022.222.132137\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eUpadhyay et al. (2018). Molecular recognition of flunarizine dihydrochloride and β-cyclodextrin inclusion complex by NMR and computational approaches. \u003cem\u003eChemistry Central Journal\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1186\/s13065-018-0395-4\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1186\/s13065-018-0395-4\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":"25g","offer_id":48085953970394,"sku":"TCI2510B672713654","price":2447000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6727.jpg?v=1768204519"},{"product_id":"tci2510b679713713","title":"TCI B6797 4294-16-0 N6-Benzyladenosine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6797 (CAS 4294-16-0) is N6-benzyladenosine, an adenosine analogue carrying a benzyl group on the exocyclic N6 nitrogen. It is widely studied as the riboside form within the N6-benzyladenine cytokinin family in plant science research. The compound also serves as an analytical standard for HPLC and mass spectrometry work and as a starting material for further nucleoside modification. AMI Scientific supplies this TCI reagent in 1 g and 5 g pack sizes for research laboratories.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMlejnek et al. (2000). Induction of apoptosis in HL-60 cells by N6-benzyladenosine. \u003cem\u003eJournal of Cellular Biochemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/(sici)1097-4644(20000401)77:1\u0026lt;6::aid-jcb2\u0026gt;3.3.co;2-v\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/(sici)1097-4644(20000401)77:1\u0026lt;6::aid-jcb2\u0026gt;3.3.co;2-v\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eŠtarha et al. (2013). N6-Benzyladenosine Derivatives as Novel N-Donor Ligands of Platinum(II) Dichlorido Complexes. \u003cem\u003eMolecules\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.3390\/molecules18066990\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.3390\/molecules18066990\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eCastiglioni et al. (2013). N6-Isopentenyladenosine and its Analogue N6-Benzyladenosine Induce Cell Cycle Arrest and Apoptosis in Bladder Carcinoma T24 Cells. \u003cem\u003eAnti-Cancer Agents in Medicinal Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.2174\/1871520611313040016\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.2174\/1871520611313040016\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":48085956559066,"sku":"TCI2510B679713713","price":2699000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085956591834,"sku":"TCI2510B679713714","price":9333000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6797.jpg?v=1769144609"},{"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":48085956788442,"sku":"TCI2510B680313719","price":2559000.0,"currency_code":"IDR","in_stock":true},{"title":"25mg","offer_id":48085956821210,"sku":"TCI2510B680313720","price":8180000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6803.jpg?v=1768816104"},{"product_id":"tci2510b683813743","title":"TCI B6838 218600-53-4 Bardoxolone Methyl","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6838 Bardoxolone Methyl (CDDO-Me, CAS 218600-53-4) is a synthetic oleanane triterpenoid widely used as a reference tool in oxidative stress and inflammation research. It is best known as a potent activator of the Keap1–Nrf2 pathway and a modulator of NF-κB-driven inflammatory signalling in cell models. Typical experiments involve preparing a DMSO stock, treating cultured cells, and measuring antioxidant response gene expression, phase II enzyme levels, or cytokine output. Supplied in a 250 mg pack, this biologically active solid should be weighed in a fume hood, stored cold and protected from light, and aliquoted to avoid repeated freeze–thaw cycles.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eYoshioka et al. (2025). Multi-Omics Reveal Antioxidant Effects of Bardoxolone Methyl in the Phase 2 Study of Bardoxolone Methyl in Patients with CKD and Type 2 Diabetes Study. \u003cem\u003eKidney360\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.34067\/kid.0000000853\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.34067\/kid.0000000853\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eKernel Networks Inc. (2019). A Clinical Pharmacology Study of Bardoxolone Methyl in Healthy Adults. \u003cem\u003eCase Medical Research\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.31525\/ct1-nct04023903\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.31525\/ct1-nct04023903\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eFu et al. (2013). Efficient and Scalable Synthesis of Bardoxolone Methyl (CDDO-methyl Ester). \u003cem\u003eOrganic Letters\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1021\/ol400399x\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1021\/ol400399x\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":"250mg","offer_id":48085957640410,"sku":"TCI2510B683813743","price":8826000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6838.jpg?v=1769144609"},{"product_id":"tci2510c000213908","title":"TCI C0002 331-39-5 Caffeic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0002 Caffeic Acid is a naturally occurring hydroxycinnamic acid found widely in coffee, fruits, vegetables, and medicinal plants. Its catechol moiety confers strong radical-scavenging and metal-chelating behavior, making it a common reference compound in antioxidant assays. It also serves as an HPLC standard for polyphenol quantification and as a useful non-heterocyclic building block for synthesis. Available in 5 g and 25 g packs, it should be stored cool, dry, and shielded from light to limit oxidative darkening.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eTosovic (2017). Spectroscopic features of caffeic acid: Theoretical study. \u003cem\u003eKragujevac Journal of Science\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.5937\/kgjsci1739099t\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.5937\/kgjsci1739099t\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eQin et al. (2021). Interaction between caffeic acid\/caffeic acid phenethyl ester and micellar casein. \u003cem\u003eFood Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.foodchem.2021.129154\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.foodchem.2021.129154\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eKhim Phin et al. (2009). In Vitro Synergy Effect of Syringic Acid, Caffeic Acid and 4-hydroxybenzoic Acid against Ganoderma boninense. \u003cem\u003eInternational Journal of Engineering and Technology\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.7763\/ijet.2009.v1.53\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.7763\/ijet.2009.v1.53\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":48085965308122,"sku":"TCI2510C000213908","price":957000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085965340890,"sku":"TCI2510C000213909","price":3177000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0002.jpg?v=1767094529"},{"product_id":"tci2510c000413911","title":"TCI C0004 154071-48-4 Calcein (mixture of isomers) [for Fluorometric Determination of Ca]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0004 Calcein (mixture of isomers) is a fluorescein-based fluorescent probe bearing iminodiacetate chelating groups. It is widely used in life science as a fluorescent label for cell studies, membrane integrity assessment, and as a bone-mineralization marker in growth-rate measurements. In analytical work it also serves as a metallofluorescent indicator for the fluorometric determination of calcium. Available in 1 g and 5 g packs, it should be protected from light and stored cool and dry to preserve fluorescence intensity.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085965406426,"sku":"TCI2510C000413911","price":1771000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085965439194,"sku":"TCI2510C000413912","price":5791000.0,"currency_code":"IDR","in_stock":true}]},{"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":507000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085965734106,"sku":"TCI2510C001013919","price":2531000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0010.jpg?v=1767094541"},{"product_id":"tci2510c001113920","title":"TCI C0011 76-22-2 (+\/-)-Camphor","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0011 (+\/-)-Camphor, CAS 76-22-2, is the racemic form of the well-known bicyclic terpenoid ketone. It is intended for applications where optical purity is not required, serving as an economical non-heterocyclic building block for general synthetic work. The reactive carbonyl group readily undergoes reduction, oximation, and condensation reactions, while its ready sublimation makes it a classic teaching material. AMI Scientific provides this TCI product in 25 g and 500 g pack sizes for research and teaching laboratories alike.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eChan et al. (2009). Status epilepticus after topical application of a solution containing camphor. \u003cem\u003eEmergency Medicine Journal\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1136\/emj.2008.063198\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1136\/emj.2008.063198\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eYE et al. (1991). ChemInform Abstract: Selective Anodic Oxidation of Camphor.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199142265\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199142265\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eSTINSON (1998). Chiral camphor carries acetate in asymmetric condensation. \u003cem\u003eChemical \u0026amp; Engineering News Archive\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1021\/cen-v076n005.p029\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1021\/cen-v076n005.p029\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":48085965799642,"sku":"TCI2510C001113920","price":507000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085965832410,"sku":"TCI2510C001113921","price":1857000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0011.jpg?v=1767094545"},{"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":2727000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0018.jpg?v=1771058480"},{"product_id":"tci2510c001913937","title":"TCI C0019 56-25-7 Cantharidin","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCantharidin, with the CAS number 56-25-7, is a chemical compound widely utilized in biochemical and pharmacological experiments. It is a potent toxin and is commonly used as a testing agent in research focused on enzyme and receptor mechanisms. As an alkaloid, its complex structure makes it a valuable subject for structure-function studies. In the laboratory, it plays a critical role in assessing cellular responses to specific stimuli, particularly in toxicity and pharmacological effect investigations. Its unique ability to elicit specific biological responses makes it an essential tool for scientific research.\u003c\/p\u003e\n\u003cp\u003eCantharidin is preferred due to its chemical stability under controlled conditions and its ability to interact with various proteins and enzymes. These properties make it an effective tool for molecular interaction studies. Despite its stability, it is highly sensitive to environmental changes, which requires careful handling and storage to maintain its integrity. Its versatility in triggering specific biological responses further enhances its value in experimental settings. Researchers rely on its predictable behavior in controlled environments to obtain reliable and reproducible results.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Cantharidin is commonly used in biochemistry and pharmacology research. It is essential for studies involving cellular toxicity, enzyme inhibition, and receptor activation. Its application is particularly relevant in academic and research institutions where biochemical experiments are conducted. The compound's role in understanding molecular interactions and biological responses makes it a key component in many scientific investigations. Its use is well-established in both teaching and research laboratories across Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBiochemical Research: Cantharidin is used to study enzyme inhibition and receptor activation, providing insights into molecular interactions.\u003c\/li\u003e\n\u003cli\u003eToxicology Studies: Its potent toxicity makes it ideal for assessing cellular responses to toxic agents and evaluating drug effects.\u003c\/li\u003e\n\u003cli\u003ePharmacological Testing: The compound is employed to investigate the mechanisms of drug action and biological responses in controlled environments.\u003c\/li\u003e\n\u003cli\u003eStructural-Functional Analysis: Its complex alkaloid structure supports research on how molecular architecture influences biological activity.\u003c\/li\u003e\n\u003cli\u003eCellular Response Evaluation: Cantharidin helps researchers analyze how cells react to specific stimuli, particularly in toxicity and pharmacological 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: 56-25-7\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 standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Crystalline solid\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCantharidin should be stored in a cool, dry place away from direct sunlight and moisture. It is recommended to use airtight containers to prevent exposure to air and humidity. Due to its sensitivity to environmental changes, it is important to maintain stable storage conditions to preserve its chemical integrity. Proper labeling and secure storage are essential to prevent accidental exposure. Laboratory personnel should wear appropriate personal protective equipment when handling this compound. Regular monitoring of storage conditions ensures that the material remains effective for research purposes.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48085966389466,"sku":"TCI2510C001913937","price":2924000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0019.jpg?v=1769144597"},{"product_id":"tci2510c007113999","title":"TCI C0071 94-41-7 Chalcone","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0071 Chalcone (CAS 94-41-7) is an α,β-unsaturated aromatic ketone that serves as a versatile building block in organic and medicinal chemistry. It is widely used as a Michael acceptor, a precursor to pyrazolines and flavanones, and a model substrate in asymmetric catalysis and photochemical studies. TCI offers the compound in a 25 g pack size suitable for routine synthetic work. Store it in a tightly closed container away from light and moisture, and handle with appropriate protective equipment.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePatil et al. (2010). ChemInform Abstract: Chalcone — A Versatile Molecule. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.201025251\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.201025251\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eLi et al. (2006). Highly Stereoselective Nitration of Chalcone Derivatives with Nitric Oxide.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.200641082\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.200641082\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eAbe et al. (2010). ChemInform Abstract: Structure and Function of the Chalcone Synthase Superfamily of Plant Type III Polyketide Synthases. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.201037269\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.201037269\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":48276755841242,"sku":"TCI2510C007113999","price":985000.0,"currency_code":"IDR","in_stock":false}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0071.jpg?v=1767094618"},{"product_id":"tci2510c007614008","title":"TCI C0076 7080-50-4 Chloramine T Trihydrate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI Chloramine T Trihydrate (catalog C0076, CAS 7080-50-4) is one of the most widely used active-chlorine reagents in the laboratory, valued for its stable solid form and easy dissolution in water. It functions both as a general oxidant in synthetic chemistry and as an electrophilic nitrogen source in carbon–nitrogen bond forming methodologies. In biochemistry and analytical work it is well known as an oxidizing reagent for protein labelling procedures and for colorimetric and titrimetric determinations. AMI Scientific supplies this TCI product in 25g and 500g pack sizes; keep it cool, dry, light-protected, and well away from acids and reducing agents.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMekky et al. (2022). Chloramine Trihydrate‐Mediated Tandem Synthesis of New Pyrrole and\/or Arene‐Linked Mono‐ and Bis(1,3,4‐Oxadiazole) Hybrids as Potential Bacterial Biofilm and MRSA Inhibitors. \u003cem\u003eChemistry \u0026amp; Biodiversity\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/cbdv.202200338\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/cbdv.202200338\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":48085969502426,"sku":"TCI2510C007614008","price":507000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085969535194,"sku":"TCI2510C007614009","price":1266000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0076.jpg?v=1769144594"},{"product_id":"tci2510c018114159","title":"TCI C0181 327-97-9 Chlorogenic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0181 Chlorogenic Acid, CAS 327-97-9, is a naturally occurring polyphenol widely studied in phytochemical and natural product research. It is frequently used as a reference compound for polyphenol quantification, antioxidant assays, and extraction method validation. AMI Scientific supplies it in 1 g and 5 g packs, suitable for pharmaceutical, food science, and biotechnology laboratories. The material is intended for research and experimental use only; store it tightly closed, protected from light and moisture, and handle it with standard laboratory protective equipment.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eWei et al. (2011). Isolation of Chlorogenic Acid from Flaveria bidentis (L.) Kuntze by CCC and Synthesis of Chlorogenic Acid-Intercalated Layered Double Hydroxide. \u003cem\u003eChromatographia\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1007\/s10337-010-1877-2\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1007\/s10337-010-1877-2\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eWeidel et al. (2014). A Rapid Method for Quantifying Chlorogenic Acid Levels in Potato Samples. \u003cem\u003eJournal of AOAC International\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.5740\/jaoacint.13-099\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.5740\/jaoacint.13-099\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eHolowinski et al. (2022). Chlorogenic acid-water complexes in chlorogenic acid containing food products. \u003cem\u003eJournal of Food Composition and Analysis\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.jfca.2022.104509\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.jfca.2022.104509\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":48085975761114,"sku":"TCI2510C018114159","price":2447000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085975793882,"sku":"TCI2510C018114160","price":8376000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0181.jpg?v=1767094840"},{"product_id":"tci2510c020614199","title":"TCI C0206 94-74-6 (4-Chloro-2-methylphenoxy)acetic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(4-Chloro-2-methylphenoxy)acetic Acid (TCI C0206, CAS 94-74-6), commonly abbreviated as MCPA, is a solid phenoxyacetic acid compound. Laboratories use it as a reference material for phenoxy herbicide residue analysis in water, soil, and agricultural samples. It is also studied in plant physiology research because of its auxin-like activity, and its phenoxyacetate scaffold can be derivatised in organic synthesis. AMI Scientific offers this TCI product in a 25 g pack for environmental, agricultural, and quality-testing laboratories in Indonesia.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48276753318106,"sku":"TCI2510C020614199","price":732000.0,"currency_code":"IDR","in_stock":false}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0206.jpg?v=1767094869"},{"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":1715000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48085989490906,"sku":"TCI2510C031514371","price":4751000.0,"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":1743000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48085989589210,"sku":"TCI2510C031614373","price":5256000.0,"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":1885000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085989654746,"sku":"TCI2510C031714375","price":6156000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48085989687514,"sku":"TCI2604C031794","price":536000.0,"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":1406000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48085989785818,"sku":"TCI2510C031814377","price":3964000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085989818586,"sku":"TCI2510C031814378","price":13773000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0318.jpg?v=1767095027"},{"product_id":"tci2510c032114381","title":"TCI C0321 604-33-1 Cholesterol Linoleate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0321 Cholesterol Linoleate (CAS 604-33-1) is the cholesteryl ester of linoleic acid, combining a rigid steroid core with a polyunsaturated acyl chain. It serves both as a component in cholesteric liquid crystal studies and as a widely used reference material in lipid research, lipid oxidation work, and lipoprotein model systems. Because of its unsaturated chain, the product is best stored cold, tightly closed, and protected from light and air. It is supplied by Tokyo Chemical Industry in a 25 g pack and should be handled with standard laboratory personal protective equipment.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMori et al. (1992). Biosynthesis of cholesterol linoleate by polyethylene glycol‐modified cholesterol esterase in organic solvents. \u003cem\u003eBiotechnology and Applied Biochemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1111\/j.1470-8744.1992.tb00209.x\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1111\/j.1470-8744.1992.tb00209.x\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eHavrilla et al. (2000). Coordination (Ag+) Ion Spray−Mass Spectrometry of Peroxidation Products of Cholesterol Linoleate and Cholesterol Arachidonate: High-Performance Liquid Chromatography−Mass Spectrometry Analysis of Peroxide Products from Polyunsaturated Lipid Autoxidation. \u003cem\u003eJournal of the American Chemical Society\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1021\/ja001180f\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1021\/ja001180f\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eBeadell et al. (2021). Nano- and Macroscale Imaging of Cholesterol Linoleate and Human Beta Defensin 2-Induced Changes in Pseudomonas aeruginosa Biofilms. \u003cem\u003eAntibiotics\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.3390\/antibiotics10111279\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.3390\/antibiotics10111279\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":48085989982426,"sku":"TCI2510C032114381","price":4751000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0321.jpg?v=1768816212"},{"product_id":"tci2510c032214382","title":"TCI C0322 601-34-3 Cholesterol Palmitate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0322 Cholesterol Palmitate (CAS 601-34-3) is a saturated cholesteryl ester used both as a liquid crystal material and as a reference compound in lipid research. Its long saturated acyl chain promotes ordered molecular packing, making it valuable for thermotropic phase studies using DSC and polarised light microscopy. In the life sciences it serves as a model cholesteryl ester for cholesterol metabolism and intracellular lipid storage investigations. Supplied by Tokyo Chemical Industry in 5 g and 25 g packs, it should be stored cool, dry, and protected from light.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48085990047962,"sku":"TCI2510C032214382","price":1041000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085990080730,"sku":"TCI2510C032214383","price":3289000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0322.jpg?v=1768816212"},{"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":1434000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085990211802,"sku":"TCI2510C032414386","price":15740000.0,"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":1827000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48085990441178,"sku":"TCI2510C032514388","price":5876000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085990473946,"sku":"TCI2510C032514389","price":19169000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0325.jpg?v=1768816214"}],"url":"https:\/\/amiscientific.com\/en\/collections\/tci-l2-cell-biology.oembed?page=12","provider":"AMI Scientific","version":"1.0","type":"link"}