You Searched For: D-(+)-Galactose

Catalog Number: (10295-326)

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.

Certificates

Catalog Number: (10100-182)

Supplier: Prosci

Description: GALM is an enzyme that catalyzes the epimerization of hexose sugars such as glucose and galactose. It is expressed in the cytoplasm and has a preference for galactose. The protein may be required for normal galactose metabolism by maintaining the equilibrium of alpha and beta anomers of galactose.

Catalog Number: (10295-328)

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: Biolegend

Description: CD301, Monoclonal Antibody, Clone: LOM-14, Host: Rat, Species Reactivity: Mouse, Isotype: IgG2b, K, Conjugate: APC/Fire 750, Immunogen: Purified and recombinant mouse MGL1 and MGL2, Other Names: MGL, M-ASGP-BP, Macrophage galactose-type C-type lectin, CLEC10A, CD301a, Size: 25 uG

Catalog Number: (103680-908)

Supplier: Sino Biological

Description: A DNA sequence encoding the human GALK1 (P51570) (Met 1-Leu 392) was fused with the N-terminal polyhistidine-tagged GST tag at the N-terminus.

Catalog Number: (10103-734)

Supplier: Prosci

Description: B3GALT6 (Beta-1,3-galactosyltransferase) transfers galactose from UDP-galactose to substrates with a terminal beta-linked galactose residue. It has a preference for galactose-beta-1,4-xylose that is found in the linker region of glycosaminoglycans, such as heparan sulfate and chondroitin sulfate. It has no activity towards substrates with terminal glucosamine or galactosamine residues.

Supplier: MP Biomedicals

Description: Raffinose is a trisaccharide composed of galactose, fructose, and glucose.

SDS Certificates

Catalog Number: (103612-370)

Supplier: Sino Biological

Description: Produced in rabbits immunized with purified, recombinant Human UDP galactose-4'-epimerase / GALE (rh UDP galactose-4'-epimerase / GALE; Catalog#14810-H07E; Q14376; Met1-Ala348). UDP galactose-4'-epimerase / GALE specific IgG was purified by Human UDP galactose-4'-epimerase / GALE affinity chromatography.

Catalog Number: (10391-146)

Supplier: Bioss

Description: GALT (Galactose 1 phosphate uridyl transferase) catalyzes the second step of the Leloir pathway of galactose metabolism, namely the conversion of UDP glucose + galactose 1 phosphate to glucose 1 phosphate + UDP galactose. The absence of this enzyme results in classic galactosemia in humans and can be fatal in the newborn period if lactose is not removed from the diet. The pathophysiology of galactosemia has not been clearly defined.

Supplier: Biolegend

Description: CD301, Monoclonal Antibody, Clone: LOM-14, Host: Rat, Species Reactivity: Mouse, Isotype: IgG2b, K, Conjugate: PE/Dazzle 594, Immunogen: Purified and recombinant mouse MGL1 and MGL2, Other Names: MGL, M-ASGP-BP, Macrophage galactose-type C-type lectin, CLEC10A, CD301a, Size: 100 uG

Catalog Number: (76010-468)

Supplier: Prosci

Description: Receptor with an affinity for galactose and fucose. Could be involved in endocytosis (By similarity).

Catalog Number: (IC11IPTG0001)

Supplier: MP Biomedicals

Description: IPTG (Isopropyl-β-D-thiogalactopyranoside) is a galactose analogue not recognized by β-galactosidase. IPTG is a non-metabolizable galactose analog that induces expression of the lac operon in Escherichia coli.

Catalog Number: (10110-102)

Supplier: Prosci

Description: Galactose-1-phosphate uridyl transferase (GALT) catalyzes the second step of the Leloir pathway of galactose metabolism, namely the conversion of UDP-glucose + galactose-1-phosphate to glucose-1-phosphate + UDP-galactose. The absence of this enzyme results in classic galactosemia in humans and can be fatal in the newborn period if lactose is not removed from the diet. The pathophysiology of galactosemia has not been clearly defined. Galactose-1-phosphate uridyl transferase (GALT) catalyzes the second step of the Leloir pathway of galactose metabolism, namely the conversion of UDP-glucose + galactose-1-phosphate to glucose-1-phosphate + UDP-galactose. The absence of this enzyme results in classic galactosemia in humans and can be fatal in the newborn period if lactose is not removed from the diet. The pathophysiology of galactosemia has not been clearly defined. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.

Catalog Number: (75790-240)

Supplier: Prosci

Description: GALK2 acts as a galactokinase when galactose is present at high concentrations

Supplier: MP Biomedicals

Description: Agarose is a linear polymer consisting of alternating D-galactose and 3,6-anhydro-L-galactose units. Agarose is a purified linear galactan hydrocolloid isolated from agar or agar-bearing marinealgae.