Sie suchten nach: L(-)-Galactose

Artikel-Nr: (BOSSBS-13267R-A647)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-13267R-A647

Beschreibung: 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.

UOM: 1 * 100 µl

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Artikel-Nr: (BOSSBS-13267R-CY7)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-13267R-CY7

Beschreibung: 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.

UOM: 1 * 100 µl

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Artikel-Nr: (BOSSBS-13267R-FITC)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-13267R-FITC

Beschreibung: 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.

UOM: 1 * 100 µl

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Lieferant: Apollo Scientific

Beschreibung: 6-Azido-6-deoxy-D-galactopyranose 98% min

Lieferant: Apollo Scientific

Beschreibung: Penta-O-acetyl-β-D-galactopyranose 98%

Artikel-Nr: (BOSSBS-8033R-CY5)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-8033R-CY5

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

UOM: 1 * 100 µl

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Lieferant: Cayman Chemical

Beschreibung: D-Galactosamine is an amino sugar derivative of D-galactose. D-Galactosamine is hepatotoxic and is used, alone or in combination with LPS, as a model of liver failure in rodents.

Lieferant: Thermo Fisher Scientific

Beschreibung: Penta-O-acetyl-β-D-galactopyranose 99+%

Sicherheitsdatenblätter

Artikel-Nr: (BOSSBS-8033R-CY7)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-8033R-CY7

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

UOM: 1 * 100 µl

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Lieferant: Thermo Fisher Scientific

Beschreibung: N-Acetyl-D-galactosamine 98%

Sicherheitsdatenblätter

Lieferant: Apollo Scientific

Beschreibung: A synthetic intermediated for oligosaccharide synthesis.

Lieferant: Thermo Fisher Scientific

Beschreibung: CAS No.: 14215-68-0

Sicherheitsdatenblätter

Artikel-Nr: (BOSSBS-13265R-A555)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-13265R-A555

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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Artikel-Nr: (BOSSBS-13265R-A350)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-13265R-A350

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: Apollo Scientific

Beschreibung: 2-Deoxy-2-fluoro-L-fucose ≥98%

Artikel-Nr: (BOSSBS-13265R-A680)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-13265R-A680

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

Sale