G6PC Polyclonal Antibody

Background:
Glucose-6-phosphatase (G6Pase) is a multi-subunit integral membrane protein of the endoplasmic reticulum that is composed of a catalytic subunit and transporters for G6P, inorganic phosphate, and glucose. This gene (G6PC) is one of the three glucose-6-phosphatase catalytic-subunit-encoding genes in human: G6PC, G6PC2 and G6PC3. Glucose-6-phosphatase catalyzes the hydrolysis of D-glucose 6-phosphate to D-glucose and orthophosphate and is a key enzyme in glucose homeostasis, functioning in gluconeogenesis and glycogenolysis. Mutations in this gene cause glycogen storage disease type I (GSD1). This disease, also known as von Gierke disease, is a metabolic disorder characterized by severe hypoglycemia associated with the accumulation of glycogen and fat in the liver and kidneys.

Research Area: Cancer, Cell Biology, Metabolism

Synonyms:
AW107337, G-6-Pase, G6Pase, G6Pase-alpha, g6pc, G6PC, G6PT, Glucose-6-phosphatase alpha, Glucose-6-phosphatase, GSD1, GSD1a, MGC163350, MGC93613, RP23-281C18.19

Immunogen: Synthetic peptide of human G6PC

Swissprot: P35575
Gene Accession: NP000142

Purification Method: Antigen affinity purification

Buffer: PBS with 0.05% NaN3 and 40% Glycerol, pH7.4

Concentration: 2.04 mg/mL
Dilution: IHC 1:70-1:350, ELISA 1:5000-1:10000

Storage:
Store at -20°C. Avoid freeze / thaw cycles.