Sie suchten nach: VARLP110717ALFA00053

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

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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-A750

UOM: 1 * 100 µl

Hersteller Artikel Nummer : BS-13265R-A750

Lieferant: Bioss

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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

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Beschreibung: Galactokinase is a major enzyme for the metabolism of galactose and its deficiency causes congenital cataracts in the adult population. GALK1 sequence shares the greatest level of conservation, 44.5% identity with that from E. coli and 34.6% amino acid identity with the product of the human GALK2 gene.

Artikel-Nr: BOSSBS-3983R

UOM: 1 * 100 µl

Hersteller Artikel Nummer : BS-3983R

Lieferant: Bioss

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Beschreibung: Galactokinase is a major enzyme for the metabolism of galactose and its deficiency causes congenital cataracts in the adult population. GALK1 sequence shares the greatest level of conservation, 44.5% identity with that from E. coli and 34.6% amino acid identity with the product of the human GALK2 gene.

Artikel-Nr: BOSSBS-3983R-CY7

UOM: 1 * 100 µl

Hersteller Artikel Nummer : BS-3983R-CY7

Lieferant: Bioss

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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-A680

UOM: 1 * 100 µl

Hersteller Artikel Nummer : BS-16215R-A680

Lieferant: Bioss

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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

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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

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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-A555

UOM: 1 * 100 µl

Hersteller Artikel Nummer : BS-7588R-A555

Lieferant: Bioss

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Beschreibung: Galactokinase is a major enzyme for the metabolism of galactose and its deficiency causes congenital cataracts in the adult population. GALK1 sequence shares the greatest level of conservation, 44.5% identity with that from E. coli and 34.6% amino acid identity with the product of the human GALK2 gene.

Artikel-Nr: BOSSBS-3983R-CY3

UOM: 1 * 100 µl

Hersteller Artikel Nummer : BS-3983R-CY3

Lieferant: Bioss

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Beschreibung: Galactokinase is a major enzyme for the metabolism of galactose and its deficiency causes congenital cataracts in the adult population. GALK1 sequence shares the greatest level of conservation, 44.5% identity with that from E. coli and 34.6% amino acid identity with the product of the human GALK2 gene.

Artikel-Nr: BOSSBS-3983R-CY5.5

UOM: 1 * 100 µl

Hersteller Artikel Nummer : BS-3983R-CY5.5

Lieferant: Bioss

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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-CY5.5

UOM: 1 * 100 µl

Hersteller Artikel Nummer : BS-7593R-CY5.5

Lieferant: Bioss

Sale

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-CY7

UOM: 1 * 100 µl

Hersteller Artikel Nummer : BS-7593R-CY7

Lieferant: Bioss

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Beschreibung: Hydrolyzes the galactose ester bonds of galactosylceramide, galactosylsphingosine, lactosylceramide, and monogalactosyldiglyceride. Enzyme with very low activity responsible for the lysosomal catabolism of galactosylceramide, a major lipid in myelin, kidney and epithelial cells of small intestine and colon.

Artikel-Nr: BOSSBS-4691R-HRP

UOM: 1 * 100 µl

Hersteller Artikel Nummer : BS-4691R-HRP

Lieferant: Bioss

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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-CY7

UOM: 1 * 100 µl

Hersteller Artikel Nummer : BS-8056R-CY7

Lieferant: Bioss

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Beschreibung: Catalyzes the transfer of sulfate to position 6 of galactose residues of keratan. It has a preference for sulfating keratan sulfate, but it also transfers sulfate to the unsulfated polymer. The sulfotransferase activity on sialyl LacNAc structures is much higher than the corresponding desialylated substrate, and only internal galactose residues are sulfated. It also may function in the sulfation of sialyl N-acetyllactosamine oligosaccharide chains attached to glycoproteins. It participates in biosynthesis of selectin ligands. Selectin ligands are present in high endothelial cells (HEVs) and play a central role in lymphocyte homing at sites of inflammation. Aggrecan is the major proteoglycan of human articular cartilage. The core protein is substituted by a number of keratan sulfate and chondroitin sulfate glycosaminoglycan chains. Whereas chondroitin sulfate is widely distributed throughout the body, keratan sulfate is primarily expressed in cartilage (joints, trachea, intervertebral discs) and cornea.

Artikel-Nr: BOSSBS-4894R-HRP

UOM: 1 * 100 µl

Hersteller Artikel Nummer : BS-4894R-HRP

Lieferant: Bioss

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