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Disodium UDP-glucose ≥90%, weißes Pulver

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

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Anti-UDP Glucose Ceramide Glucosyltransferase Rabbit Polyclonal Antibody

Artikel-Nr: (USBI142720-50)
Lieferant: US Biological
Hersteller Artikel Nummer : 142720-50
Beschreibung: Anti-UDP Glucose Ceramide Glucosyltransferase Rabbit Polyclonal Antibody
UOM: 1 * 50 µG

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Anti-UGP2 Rabbit Polyclonal Antibody (Cy7®)

Artikel-Nr: (BOSSBS-4043R-CY7)
Lieferant: Bioss
Hersteller Artikel Nummer : BS-4043R-CY7
Beschreibung: 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
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Anti-UGP2 Rabbit Polyclonal Antibody (Alexa Fluor® 488)

Artikel-Nr: (BOSSBS-4043R-A488)
Lieferant: Bioss
Hersteller Artikel Nummer : BS-4043R-A488
Beschreibung: 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
Image Unavailable-BOSSBS-4043R-A680

Anti-UGP2 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Artikel-Nr: (BOSSBS-4043R-A680)
Lieferant: Bioss
Hersteller Artikel Nummer : BS-4043R-A680
Beschreibung: 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
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Anti-UGP2 Rabbit Polyclonal Antibody

Artikel-Nr: (BOSSBS-4043R)
Lieferant: Bioss
Hersteller Artikel Nummer : BS-4043R
Beschreibung: 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
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Anti-UGP2 Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Artikel-Nr: (BOSSBS-4043R-A350)
Lieferant: Bioss
Hersteller Artikel Nummer : BS-4043R-A350
Beschreibung: 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
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Anti-UGP2 Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Artikel-Nr: (BOSSBS-4043R-A555)
Lieferant: Bioss
Hersteller Artikel Nummer : BS-4043R-A555
Beschreibung: 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
Image Unavailable-BOSSBS-4043R-A750

Anti-UGP2 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Artikel-Nr: (BOSSBS-4043R-A750)
Lieferant: Bioss
Hersteller Artikel Nummer : BS-4043R-A750
Beschreibung: 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
Image Unavailable-BOSSBS-4043R-CY5

Anti-UGP2 Rabbit Polyclonal Antibody (Cy5®)

Artikel-Nr: (BOSSBS-4043R-CY5)
Lieferant: Bioss
Hersteller Artikel Nummer : BS-4043R-CY5
Beschreibung: 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
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Anti-GYG1 Rabbit Polyclonal Antibody (Cy7®)

Artikel-Nr: (BOSSBS-13447R-CY7)
Lieferant: Bioss
Hersteller Artikel Nummer : BS-13447R-CY7
Beschreibung: 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
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Anti-UGP2 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Artikel-Nr: (BOSSBS-4043R-FITC)
Lieferant: Bioss
Hersteller Artikel Nummer : BS-4043R-FITC
Beschreibung: 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
Image Unavailable-BOSSBS-13447R-FITC

Anti-GYG1 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Artikel-Nr: (BOSSBS-13447R-FITC)
Lieferant: Bioss
Hersteller Artikel Nummer : BS-13447R-FITC
Beschreibung: 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
Image Unavailable-BOSSBS-13265R-A555

Anti-GALE Rabbit Polyclonal Antibody (Alexa Fluor® 555)

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
Image Unavailable-BOSSBS-13265R-A350

Anti-GALE Rabbit Polyclonal Antibody (Alexa Fluor® 350)

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
Image Unavailable-BOSSBS-13265R-A680

Anti-GALE/Galactowaldenase Rabbit Polyclonal Antibody (Alexa Fluor® 680)

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
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