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alpha-GalNAc-N3 alpha-GalNAc-N3, a prominent biomedicine extensively utilized in the pharmaceutical industry, stands as an indispensable chemical probe or precursor for synthesizing glycan-modified biomolecules. Boasting the remarkable attribute of azide functionality, it offers a powerful avenue to incorporate GalNAc moieties into targeted glycoproteins. Molecular formula: C10H18N4O6. Mole weight: 290.27. BOC Sciences
alpha-GalNAc-TEG-Alkyne alpha-GalNAc-TEG-Alkyne is a crucial product in biomedicine used for the efficient delivery of therapeutic drugs targeting diseases such as cancer and viral infections. Its unique structure allows for specific and precise targeting, enabling the drugs to effectively bind to specific receptors and exert their therapeutic effects. This product plays a vital role in improving drug efficacy and minimizing off-target effects, making it an invaluable tool in the biomedical industry. Molecular formula: C17H29NO9. Mole weight: 391.41. BOC Sciences
alpha-GalNAc-TEG-COOH alpha-GalNAc-TEG-COOH is a paramount biomedical compound widely employed in drug delivery systems, serving as an instrumental component in research and development of innovative therapeutic approaches, offering targeted drug delivery for the research of a myriad of afflictions. Molecular formula: C17H31NO11. Mole weight: 425.53. BOC Sciences
alpha-GalNAc-TEG-N3 Alpha-GalNAc-TEG-N3 is an indispensable compound, playing a pivotal role in the precise transportation of pharmaceuticals to designated cells. By virtue of its unparalleled characteristics, it serves as a catalyst for effectively administering therapeutic drugs, encompassing compounds and siRNA. Synonyms: N-[(2S,3R,4R,5R,6R)-2-[2-[2-(2-Azidoethoxy)ethoxy]ethoxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]acetamide. CAS No. 882873-70-3. Molecular formula: C14H26N4O8. Mole weight: 378.38. BOC Sciences
alpha-GalNAc-TEG-N3 CuAAC & SPAAC Click Reactions. Group: Azides. CAS No. 882873-70-3. Molecular formula: C14H26N4O8. Mole weight: 378.38. Appearance: Solid. Purity: 99%+. Catalog: CCR882873703. Alfa Chemistry. 2
β-1,3-galactosyltransferase from Campylobacter jejuni, Recombinant Beta-1,3-galactosyltransferase that transfers galactose from UDP-galactose to substrates with a terminal beta-N-acetylglucosamine (beta-GlcNAc) residue. Can also utilize substrates with a terminal galactose residue, albeit with lower efficiency. Involved in the biosynthesis of the carbohydrate moieties of glycolipids and glycoproteins. Inactive towards substrates with terminal alpha-N-acetylglucosamine (alpha-GlcNAc) or alpha-N-acetylgalactosamine (alpha-GalNAc) residues. Group: Enzymes. Synonyms: UDP-galactose-ceramide galactosyltransferase; uridine diphosphogalactose-ceramide galactosyltransferase; UDP galactose-LAC Tet-ceramide α-galactosyltransferase; UDP-galactose-GM2 galactosyltransferase; uridine diphosphogalactose-GM2 galactosyltransferase; GM1-synthase; ganglio. Enzyme Commission Number: EC 2.4.1.62. CAS No. 37217-28-0. Purity: min 95% by SDS-PAGE. Galactosyltransferase. Source: E. coli. Species: Campylobacter jejuni. UDP-galactose-ceramide galactosyltransferase; uridine diphosphogalactose-ceramide galactosyltransferase; UDP galactose-LAC Tet-ceramide α-galactosyltransferase; UDP-galactose-GM2 galactosyltransferase; uridine diphosphogalactose-GM2 galactosyltransferase; GM1-synthase; ganglioside galactosyltransferase; EC 2.4.1.62; β-1,3-galactosyltransferase; CgtB. Cat No: NATE-1488. Creative Enzymes

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