You Searched For: D-(+)-Galactose

Supplier: Ambeed

Description: 2,3,4,6-Tetra-O-acetyl-α-D-galactopyranosyl bromide 95% stabilized

New Product

Supplier: AFG Bioscience

Description: 1,3,4,6-Tetra-O-acetyl-2-azido-2-deoxy-D-galactopyranose

Supplier: Bon Opus Biosciences

Description: It offers quality recombinant proteins products covering a broad collection of cytokines, enzymes, diagnostic and detection reagents, and other protein-related products.

Catalog Number: (100268-770)

Supplier: Indofine Chemical Company

Description: Rare Organics & BioChemicals 3615-37-0 1gm 6-Deoxy-D-galactose 164.17 Room temperature.

Supplier: Ambeed

Description: Uridine-5′-diphosphogalactose disodium salt ≥98%

New Product

Supplier: ALADDIN SCIENTIFIC

Description: 2,3,4,6-Tetra-O-acetyl-α-D-galactopyranosyl bromide is used as an organic condensation reagent for chemistries such as N- and S- galactosylation reactions and the synthesis of spacer-equipped phosphorylated di-, tri- and tetrasaccharide fragments of the O-specific polysaccharides.

New Product

Supplier: Bon Opus Biosciences

Description: Bon Opus Biosciences offers quality recombinant proteins products covering a broad collection of cytokines, enzymes, diagnostic and detection reagents, and other protein-related products

Supplier: New England Biolabs (NEB)

Description: β1-4 Galactosidase S is a highly specific exoglycosidase that catalyzes the hydrolysis of β1-4 linked galactose residues from oligosaccharides.

Catalog Number: (89321-650)

Supplier: Genetex

Description: Purity: Purified by antigen-affinity chromatography. Species Reactivity: Human Tested Applications: WB Pkg Size: 100 ul

Catalog Number: (89324-784)

Supplier: Genetex

Description: Purity: Purified by antigen-affinity chromatography. Species Reactivity: Human Tested Applications: WB Pkg Size: 100 ul

Catalog Number: (76012-440)

Supplier: Prosci

Description: This gene encodes a member of the galactose-3-O-sulfotransferase protein family. The product of this gene catalyzes sulfonation by transferring a sulfate to the C-3' position of galactose residues in O-linked glycoproteins. This enzyme is highly specific for core 1 structures, with asialofetuin, Gal-beta-1,3-GalNAc and Gal-beta-1,3 (GlcNAc-beta-1,6)GalNAc being good substrates.

Catalog Number: (10295-334)

Supplier: Bioss

Description: GALE is a 348 amino acid protein that functions as the third enzyme in the Leloir pathway of galactose metabolism. A member of the sugar epimerase family, GALE exists as a homodimer, binds FAD as a cofactor and catalyzes the epimerization of UDP-N-acetylglucosamine to UDP-N-acetylgalactosamine and UDP-glucose to UDP-galactose. The gene encoding GALE maps to human chromosome 1p36.11 and mutations in this gene lead to the development of complex disorder known as epimerase-deficiency galactosemia (EDG) or galactosemia type 3, which is characterized by mental retardation, liver damage, cataracts and deafness.

Catalog Number: (76010-796)

Supplier: Prosci

Description: Galactocerebrosides are abundant sphingolipids of the myelin membrane of the central nervous system and peripheral nervous system and are also present in small amounts in kidney. The key enzymatic step in the biosynthesis of galactocerebrosides consists of the transfer of galactose to ceramide catalyzed by UDP-galactose ceramide galactosyltransferase (CGT, EC 2.4.1.45). The enzyme encoded by the CGT gene is the first involved in complex lipid biosynthesis in the myelinating oligodendrocyte.[supplied by OMIM].

Catalog Number: (10284-394)

Supplier: Bioss

Description: GALE is a 348 amino acid protein that functions as the third enzyme in the Leloir pathway of galactose metabolism. A member of the sugar epimerase family, GALE exists as a homodimer, binds FAD as a cofactor and catalyzes the epimerization of UDP-N-acetylglucosamine to UDP-N-acetylgalactosamine and UDP-glucose to UDP-galactose. The gene encoding GALE maps to human chromosome 1p36.11 and mutations in this gene lead to the development of complex disorder known as epimerase-deficiency galactosemia (EDG) or galactosemia type 3, which is characterized by mental retardation, liver damage, cataracts and deafness.

Catalog Number: (10295-330)

Supplier: Bioss

Description: GALE is a 348 amino acid protein that functions as the third enzyme in the Leloir pathway of galactose metabolism. A member of the sugar epimerase family, GALE exists as a homodimer, binds FAD as a cofactor and catalyzes the epimerization of UDP-N-acetylglucosamine to UDP-N-acetylgalactosamine and UDP-glucose to UDP-galactose. The gene encoding GALE maps to human chromosome 1p36.11 and mutations in this gene lead to the development of complex disorder known as epimerase-deficiency galactosemia (EDG) or galactosemia type 3, which is characterized by mental retardation, liver damage, cataracts and deafness.

Supplier: MP Biomedicals

Description: Uridine-5'-diphosphogalactose Disodium Salt is a donor substrate for galactosyltransferases involved in the addition of galatose (galactosylation) molecules to N-linked and O-linked oligosaccharides and glycerolipids (biosynthesis of galactose-containing oligosaccharides).
UDP-Gal and its analogues are used to study the distribution, specificity and kinetics of galactosyltransferase(s).
Store at -0 °C, desiccate.

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