You Searched For: D-(+)-Galactose


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Catalog Number: (10293-908)
Supplier: Bioss
Description: GALK2 is important in the first step of the galactose metabolism pathway. GALK1, which belongs to the GHMP kinase family of proteins, is a crucial enzyme for galactose metabolism, specifically converting ?d-galactose to galactose 1-phosphate. Defects in the gene encoding GALK1 can cause galactosemia II, an autosomal recessive disorder characterized by congenital cataracts during infancy, often within the first two weeks of life. In the adult population, galactosemia II can cause presenile cataracts that are secondary to accumulation of galactitol in the lens of the eye. A second gene, GALK2, encodes an enzyme with greater activity against GalNAc than galactose. GALK2 has been implicated in the salvage pathway for the reutilization of free GalNAc derived from the degradation of complex carbohydrates.


Catalog Number: (89267-904)
Supplier: Genetex
Description: Rabbit polyclonal antibody to GALM (Middle)


Supplier: VWR
Description: A solidifying agent used in bacteriology. Agar consists of unbranched polysaccharides of galactose subunits derived from algae or seaweed.
Catalog Number: (76073-362)
Supplier: Prosci
Description: For WB starting dilution is: 1:1000


Catalog Number: (10293-904)
Supplier: Bioss
Description: GALK2 is important in the first step of the galactose metabolism pathway. GALK1, which belongs to the GHMP kinase family of proteins, is a crucial enzyme for galactose metabolism, specifically converting ?d-galactose to galactose 1-phosphate. Defects in the gene encoding GALK1 can cause galactosemia II, an autosomal recessive disorder characterized by congenital cataracts during infancy, often within the first two weeks of life. In the adult population, galactosemia II can cause presenile cataracts that are secondary to accumulation of galactitol in the lens of the eye. A second gene, GALK2, encodes an enzyme with greater activity against GalNAc than galactose. GALK2 has been implicated in the salvage pathway for the reutilization of free GalNAc derived from the degradation of complex carbohydrates.


Catalog Number: (77438-598)
Supplier: Bioss
Description: Mutarotase converts alpha-aldose to the beta-anomer. It is active on D-glucose, L-arabinose, D-xylose, D-galactose, maltose and lactose.


Supplier: Thermo Scientific Chemicals
Description: Mucin is used in a study to investigate a galactose-specific lectin from the red marine alga <i>Ptilota filicina</i>.
Supplier: MP Biomedicals
Description: Raffinose is a trisaccharide composed of galactose, fructose, and glucose that is used as carbon source in yeast culture media.

Catalog Number: (75789-532)
Supplier: Prosci
Description: beta Galactosidase is a lysosomal beta Galactosidase that hydrolyzes the terminal beta Galactose from Ganglioside and Keratan sulfate


Catalog Number: (76073-042)
Supplier: Prosci
Description: For WB starting dilution is: 1:1000 For IHC-P starting dilution is: 1:50~100 For FACS starting dilution is: 1:10~50 For IF starting dilution is: 1:10~50


Catalog Number: (10293-912)
Supplier: Bioss
Description: GALK2 is important in the first step of the galactose metabolism pathway. GALK1, which belongs to the GHMP kinase family of proteins, is a crucial enzyme for galactose metabolism, specifically converting ?d-galactose to galactose 1-phosphate. Defects in the gene encoding GALK1 can cause galactosemia II, an autosomal recessive disorder characterized by congenital cataracts during infancy, often within the first two weeks of life. In the adult population, galactosemia II can cause presenile cataracts that are secondary to accumulation of galactitol in the lens of the eye. A second gene, GALK2, encodes an enzyme with greater activity against GalNAc than galactose. GALK2 has been implicated in the salvage pathway for the reutilization of free GalNAc derived from the degradation of complex carbohydrates.


Catalog Number: (10103-692)
Supplier: Prosci
Description: GAL3ST3 is a member of the galactose-3-O-sulfotransferase protein family. It catalyzes sulfonation by transferring a sulfate group to the 3' position of galactose in N-acetyllactosamine in both type 2 (Gal-beta-1-4GlcNAc-R) oligosaccharides and core-2-branched O-glycans, but not on type 1 or core-1-branched structures. This gene, which has also been referred to as GAL3ST2, is different from the GAL3ST2 gene located on chromosome 2 that encodes a related enzyme with distinct tissue distribution and substrate specificities, compared to galactose-3-O-sulfotransferase 3.This gene encodes a member of the galactose-3-O-sulfotransferase protein family. The product of this gene catalyzes sulfonation by transferring a sulfate group to the 3' position of galactose in N-acetyllactosamine in both type 2 (Gal-beta-1-4GlcNAc-R) oligosaccharides and core-2-branched O-glycans, but not on type 1 or core-1-branched structures. This gene, which has also been referred to as GAL3ST2, is different from the GAL3ST2 gene located on chromosome 2 that encodes a related enzyme with distinct tissue distribution and substrate specificities, compared to galactose-3-O-sulfotransferase 3.


Catalog Number: (10792-604)
Supplier: Genetex
Description: Rabbit Polyclonal antibody to GALT


Catalog Number: (MSPP-PAJ076HU1)
Supplier: CLOUD-CLONE CORP MS
Description: Polyclonal Antibody to Galactose-3-O-Sulfotransferase 1 (GAL3ST1), derived from recombinant GAL3ST1 (Leu57~Phe196), is reactive with Human/Mouse.

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Catalog Number: (89268-236)
Supplier: Genetex
Description: Rabbit polyclonal antibody to GAL3ST3 (C-terminal)


Catalog Number: (89267-906)
Supplier: Genetex
Description: Rabbit polyclonal antibody to GALM (N-terminal)


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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at 1-800-932-5000.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at Regulatory_Affairs@vwr.com
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