You Searched For: D(+)-Galactose


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Catalog Number: (BOSSBS-7588R-A488)
Supplier: Bioss
Description: Necessary for the biosynthesis of the Pk antigen of blood histogroup P. Catalyzes the transfer of galactose to lactosylceramide and galactosylceramide. Necessary for the synthesis of the receptor for bacterial verotoxins.
UOM: 1 * 100 µl


Catalog Number: (BOSSBS-7588R-A750)
Supplier: Bioss
Description: Necessary for the biosynthesis of the Pk antigen of blood histogroup P. Catalyzes the transfer of galactose to lactosylceramide and galactosylceramide. Necessary for the synthesis of the receptor for bacterial verotoxins.
UOM: 1 * 100 µl


Catalog Number: (BOSSBS-7588R-HRP)
Supplier: Bioss
Description: Necessary for the biosynthesis of the Pk antigen of blood histogroup P. Catalyzes the transfer of galactose to lactosylceramide and galactosylceramide. Necessary for the synthesis of the receptor for bacterial verotoxins.
UOM: 1 * 100 µl


Supplier: Merck
Description: D-(+)-Galactose, Millipore®

Supplier: G-Biosciences
Description: Jacalin, or <i>Artocarpus integrifolia</i> lectin, is a tetrameric two-chain lectin with a molecular weight of 66 kDa. It is a α-D-galactose binding lectin purified from jack fruit (<i>Artocarpus integrifolia</i>) seeds.

Catalog Number: (BOSSBS-13265R-CY7)
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.
UOM: 1 * 100 µl


Supplier: Thermo Fisher Scientific
Description: 1,2:3,4-Di-O-isopropylidene-ɑ-D-galactopyranose 95%
Supplier: Thermo Fisher Scientific
Description: Appearance: Clear colorless to yellow Viscous liquid or paste

SDS

Catalog Number: (BOSSBS-8033R-A750)
Supplier: Bioss
Description: Lectin that binds to various sugars: galactose > mannose = fucose > N-acetylglucosamine > N-acetylgalactosamine.
UOM: 1 * 100 µl


Supplier: Thermo Fisher Scientific
Description: 2,3,4,6-Tetra-O-benzyl-D-galactopyranose ≥98%

SDS

Catalog Number: (BOSSBS-7588R-A680)
Supplier: Bioss
Description: Necessary for the biosynthesis of the Pk antigen of blood histogroup P. Catalyzes the transfer of galactose to lactosylceramide and galactosylceramide. Necessary for the synthesis of the receptor for bacterial verotoxins.
UOM: 1 * 100 µl


Supplier: Serva
Description: D-(+)-Galactose

Supplier: Thermo Fisher Scientific
Description: D-(+)-Galactose ≥99%

Catalog Number: (BOSSBS-7593R-A488)
Supplier: Bioss
Description: Galactosidase alpha is involved in the hydrolysis of terminal, non reducing alpha D galactose residues in alpha D galactosides, including galactose oligosaccharides, galactomannans and galactohydrolase. Defects in GLA are the cause of Fabry's disease (FD). FD is a rare X-linked sphingolipidosis disease where glycolipid accumulates in many tissues. Clinical recognition in males results from characteristic skin lesions (angiokeratomas) over the lower trunk. Patients may show ocular deposits, febrile episodes, and burning pain in the extremities. Death results from renal failure, cardiac or cerebral complications of hypertension or other vascular disease. Heterozygous females may exhibit the disorder in an attenuated form, they are more likely to show corneal opacities.
UOM: 1 * 100 µl


Catalog Number: (3455-100)
Supplier: Merck Millipore (Calbiochem‎)
Description: D-(+)-Galactose, Millipore®
UOM: 1 * 100 g

Catalog Number: (BOSSBS-8033R-CY3)
Supplier: Bioss
Description: Lectin that binds to various sugars: galactose >mannose = fucose >N-acetylglucosamine >N-acetylgalactosamine.
UOM: 1 * 100 µl


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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 on 0800 22 33 44
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Additional Documentation may be needed to purchase this item. A VWR representative will contact you if needed.
This product has been blocked by your organisation. Please contact your purchasing department for more information.
The original product is no longer available. The replacement shown is available.
Product(s) marked with this symbol are discontinued - sold till end of stock. Alternatives may be available by searching with the VWR Catalogue Number listed above. If you need further assistance, please call VWR Customer Service on 0800 22 33 44.
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