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Beschreibung: 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.
Artikel-Nr: BOSSBS-7588R-CY5
UOM: 1 * 100 µl
Hersteller Artikel Nummer : BS-7588R-CY5
Lieferant: Bioss


Beschreibung: 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.
Artikel-Nr: BOSSBS-13265R-CY7
UOM: 1 * 100 µl
Hersteller Artikel Nummer : BS-13265R-CY7
Lieferant: Bioss


Beschreibung: Appearance: Clear colorless to yellow Viscous liquid or paste
Artikel-Nr: ACRO115240050
UOM: 1 * 5 g
Hersteller Artikel Nummer : 115240050
Lieferant: Thermo Fisher Scientific

Beschreibung: 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.
Artikel-Nr: BOSSBS-7588R-CY5.5
UOM: 1 * 100 µl
Hersteller Artikel Nummer : BS-7588R-CY5.5
Lieferant: Bioss


Beschreibung: 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.
Artikel-Nr: BOSSBS-7593R-A350
UOM: 1 * 100 µl
Hersteller Artikel Nummer : BS-7593R-A350
Lieferant: Bioss


Beschreibung: 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.
Artikel-Nr: BOSSBS-7593R-A488
UOM: 1 * 100 µl
Hersteller Artikel Nummer : BS-7593R-A488
Lieferant: Bioss


Beschreibung: Lectin that binds to various sugars: galactose >mannose = fucose >N-acetylglucosamine >N-acetylgalactosamine.
Artikel-Nr: BOSSBS-8033R-CY3
UOM: 1 * 100 µl
Hersteller Artikel Nummer : BS-8033R-CY3
Lieferant: Bioss


Beschreibung: 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.
Artikel-Nr: BOSSBS-7588R-A680
UOM: 1 * 100 µl
Hersteller Artikel Nummer : BS-7588R-A680
Lieferant: Bioss


Beschreibung: 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.
Artikel-Nr: BOSSBS-7588R-A647
UOM: 1 * 100 µl
Hersteller Artikel Nummer : BS-7588R-A647
Lieferant: Bioss


Beschreibung: 1,3,4,6-Tetra-O-acetyl-2-azido-2-deoxy-D-galactopyranose ≥98%
Artikel-Nr: APOSBICL4261-500MG
UOM: 1 * 500 mg
Hersteller Artikel Nummer : BICL4261-500MG
Lieferant: Apollo Scientific


Beschreibung: KLHL14 is a member of the KLHL family. The kelch motif was initially discovered in Kelch. In this protein there are six copies of the motif. It has been shown for one member that it is related to Galactose Oxidase for which a structure has been solved. Two isoforms of this protein exist - 70kDa and 43kDa.
Artikel-Nr: BOSSBS-8056R
UOM: 1 * 100 µl
Hersteller Artikel Nummer : BS-8056R
Lieferant: Bioss


Beschreibung: KLHL14 is a member of the KLHL family. The kelch motif was initially discovered in Kelch. In this protein there are six copies of the motif. It has been shown for one member that it is related to Galactose Oxidase for which a structure has been solved. Two isoforms of this protein exist - 70kDa and 43kDa.
Artikel-Nr: BOSSBS-8056R-CY5
UOM: 1 * 100 µl
Hersteller Artikel Nummer : BS-8056R-CY5
Lieferant: Bioss


Beschreibung: D(+)-Galactose
Artikel-Nr: WAKO075-00035
UOM: 1 * 500 g
Hersteller Artikel Nummer : 075-00035
Lieferant: Wako


Beschreibung: Catalyses the transfer of sulfate to beta-1,3-linked galactose residues in O-linked glycoproteins. Good substrates include asialofetuin, Gal-beta-1,3-GalNAc and Gal-beta-1,3 (GlcNAc-beta-1,6)GalNAc.
Artikel-Nr: BOSSBS-16215R-A750
UOM: 1 * 100 µl
Hersteller Artikel Nummer : BS-16215R-A750
Lieferant: Bioss


Beschreibung: 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.
Artikel-Nr: BOSSBS-7593R-A680
UOM: 1 * 100 µl
Hersteller Artikel Nummer : BS-7593R-A680
Lieferant: Bioss


Beschreibung: Lectin that binds to various sugars: galactose >mannose = fucose >N-acetylglucosamine >N-acetylgalactosamine.
Artikel-Nr: BOSSBS-8033R-A647
UOM: 1 * 100 µl
Hersteller Artikel Nummer : BS-8033R-A647
Lieferant: Bioss


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