Du søkte etter: Disodium+UDP-glucose

Produsent: MP Biomedicals

Beskrivelse: Uridine-5'-diphosphoglucose Disodium Salt is a biosynthetic product produced by the reaction of UTP and glucose-1-phosphate catalysed by uridyl transferase.

Artikkenummer: (USBI142720-50)

Produsent: US Biological

Beskrivelse: Anti-UDP Glucose Ceramide Glucosyltransferase Rabbit Polyclonal Antibody

UOM: 1 * 1 Each

Tilbud

Artikkenummer: (BOSSBS-4043R-A488)

Produsent: Bioss

Beskrivelse: UGP2 (UDP glucose pyrophosphorylase 2) is an important intermediary in cellular metabolic pathways. It transfers a glucose moiety from glucose-1-phosphate to MgUTP and forms UDP glucose and MgPPi.

UOM: 1 * 100 µl

Tilbud

Artikkenummer: (BOSSBS-4043R-CY7)

Produsent: Bioss

Beskrivelse: UGP2 (UDP glucose pyrophosphorylase 2) is an important intermediary in cellular metabolic pathways. It transfers a glucose moiety from glucose-1-phosphate to MgUTP and forms UDP glucose and MgPPi.

UOM: 1 * 100 µl

Tilbud

Artikkenummer: (BOSSBS-4043R-A680)

Produsent: Bioss

Beskrivelse: UGP2 (UDP glucose pyrophosphorylase 2) is an important intermediary in cellular metabolic pathways. It transfers a glucose moiety from glucose-1-phosphate to MgUTP and forms UDP glucose and MgPPi.

UOM: 1 * 100 µl

Tilbud

Artikkenummer: (BOSSBS-4043R-A350)

Produsent: Bioss

Beskrivelse: UGP2 (UDP glucose pyrophosphorylase 2) is an important intermediary in cellular metabolic pathways. It transfers a glucose moiety from glucose-1-phosphate to MgUTP and forms UDP glucose and MgPPi.

UOM: 1 * 100 µl

Tilbud

Artikkenummer: (BOSSBS-4043R)

Produsent: Bioss

Beskrivelse: UGP2 (UDP glucose pyrophosphorylase 2) is an important intermediary in cellular metabolic pathways. It transfers a glucose moiety from glucose-1-phosphate to MgUTP and forms UDP glucose and MgPPi.

UOM: 1 * 100 µl

Tilbud

Artikkenummer: (BOSSBS-4043R-A555)

Produsent: Bioss

Beskrivelse: UGP2 (UDP glucose pyrophosphorylase 2) is an important intermediary in cellular metabolic pathways. It transfers a glucose moiety from glucose-1-phosphate to MgUTP and forms UDP glucose and MgPPi.

UOM: 1 * 100 µl

Tilbud

Artikkenummer: (BOSSBS-4043R-A750)

Produsent: Bioss

Beskrivelse: UGP2 (UDP glucose pyrophosphorylase 2) is an important intermediary in cellular metabolic pathways. It transfers a glucose moiety from glucose-1-phosphate to MgUTP and forms UDP glucose and MgPPi.

UOM: 1 * 100 µl

Tilbud

Artikkenummer: (BOSSBS-13447R-FITC)

Produsent: Bioss

Beskrivelse: Glycogen synthesis is initiated by the autoglucosylation of Glycogenin-1. Specifically, Glycogenin-1 glucosylates itself to begin the synthesis of glycogen in mammalian skeletal muscle. It acts as the primer to which further glucose monomers may be added. All of the Glycogenin-1 molecules contain at least one glucosyl residue before autoglucosylation begins. The first step of the glycogen synthesis occurs when a glucose molecule from UDP-glucose binds to the hydroxyl group of Tyr 194 on the Glycogenin-1 molecule. Using its glucosyltransferase activity, Glycogenin-1 adds more glucoses, each one coming from UDP-glucose. The glycosylation process reaches a plateau when five new glucose residues have been added, at which point glycogen synthase (GS) takes over and further elongates the chain. Glycogenin-1 remains covalently attached to the reducing end of the glycogen molecule.

UOM: 1 * 100 µl

Tilbud

Artikkenummer: (BOSSBS-3984R)

Produsent: Bioss

Beskrivelse: GALT (Galactose 1 phosphate uridyl transferase) catalyzes the second step of the Leloir pathway of galactose metabolism, namely the conversion of UDP glucose + galactose 1 phosphate to glucose 1 phosphate + UDP galactose. The absence of this enzyme results in classic galactosemia in humans and can be fatal in the newborn period if lactose is not removed from the diet. The pathophysiology of galactosemia has not been clearly defined.

UOM: 1 * 100 µl

Tilbud

Artikkenummer: (BOSSBS-4043R-CY5)

Produsent: Bioss

Beskrivelse: UGP2 (UDP glucose pyrophosphorylase 2) is an important intermediary in cellular metabolic pathways. It transfers a glucose moiety from glucose-1-phosphate to MgUTP and forms UDP glucose and MgPPi.

UOM: 1 * 100 µl

Tilbud

Artikkenummer: (BOSSBS-13447R-CY7)

Produsent: Bioss

Beskrivelse: Glycogen synthesis is initiated by the autoglucosylation of Glycogenin-1. Specifically, Glycogenin-1 glucosylates itself to begin the synthesis of glycogen in mammalian skeletal muscle. It acts as the primer to which further glucose monomers may be added. All of the Glycogenin-1 molecules contain at least one glucosyl residue before autoglucosylation begins. The first step of the glycogen synthesis occurs when a glucose molecule from UDP-glucose binds to the hydroxyl group of Tyr 194 on the Glycogenin-1 molecule. Using its glucosyltransferase activity, Glycogenin-1 adds more glucoses, each one coming from UDP-glucose. The glycosylation process reaches a plateau when five new glucose residues have been added, at which point glycogen synthase (GS) takes over and further elongates the chain. Glycogenin-1 remains covalently attached to the reducing end of the glycogen molecule.

UOM: 1 * 100 µl

Tilbud

Artikkenummer: (BOSSBS-13265R-A555)

Produsent: Bioss

Beskrivelse: 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

Tilbud

Artikkenummer: (BOSSBS-13265R-A350)

Produsent: Bioss

Beskrivelse: 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

Tilbud

Artikkenummer: (BOSSBS-13265R-A680)

Produsent: Bioss

Beskrivelse: 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

Tilbud