Sie suchten nach: L(-)-Galactose

Artikel-Nr: (BOSSBS-7588R-CY5)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-7588R-CY5

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.

UOM: 1 * 100 µl

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Artikel-Nr: (BOSSBS-13265R-CY7)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-13265R-CY7

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.

UOM: 1 * 100 µl

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Lieferant: Thermo Fisher Scientific

Beschreibung: Appearance: Clear colorless to yellow Viscous liquid or paste

Sicherheitsdatenblätter

Artikel-Nr: (BOSSBS-7588R-CY5.5)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-7588R-CY5.5

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.

UOM: 1 * 100 µl

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Artikel-Nr: (BOSSBS-7593R-A350)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-7593R-A350

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.

UOM: 1 * 100 µl

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Artikel-Nr: (BOSSBS-7593R-A488)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-7593R-A488

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.

UOM: 1 * 100 µl

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Artikel-Nr: (BOSSBS-8033R-CY3)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-8033R-CY3

Beschreibung: Lectin that binds to various sugars: galactose >mannose = fucose >N-acetylglucosamine >N-acetylgalactosamine.

UOM: 1 * 100 µl

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Artikel-Nr: (BOSSBS-7588R-A680)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-7588R-A680

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.

UOM: 1 * 100 µl

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Artikel-Nr: (BOSSBS-7588R-A647)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-7588R-A647

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.

UOM: 1 * 100 µl

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Lieferant: Apollo Scientific

Beschreibung: 1,3,4,6-Tetra-O-acetyl-2-azido-2-deoxy-D-galactopyranose ≥98%

Artikel-Nr: (BOSSBS-8056R)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-8056R

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.

UOM: 1 * 100 µl

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Artikel-Nr: (BOSSBS-8056R-CY5)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-8056R-CY5

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.

UOM: 1 * 100 µl

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Artikel-Nr: (WAKO075-00035)

Lieferant: Wako

Hersteller Artikel Nummer : 075-00035

Beschreibung: D(+)-Galactose

UOM: 1 * 500 g

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Artikel-Nr: (BOSSBS-16215R-A750)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-16215R-A750

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.

UOM: 1 * 100 µl

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Artikel-Nr: (BOSSBS-7593R-A680)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-7593R-A680

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.

UOM: 1 * 100 µl

Sale

Artikel-Nr: (BOSSBS-8033R-A647)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-8033R-A647

Beschreibung: Lectin that binds to various sugars: galactose >mannose = fucose >N-acetylglucosamine >N-acetylgalactosamine.

UOM: 1 * 100 µl

Sale