G6PC Polyclonal Antibody (E-AB-18169)

For research use only.
Verified Samples |
Verified Samples in IHC: Human liver cancer |
Dilution | IHC 1:50-1:300 |
Isotype | IgG |
Host | Rabbit |
Reactivity | Human, Mouse, Rat |
Applications | IHC |
Clonality | Polyclonal |
Immunogen | Synthetic peptide of human G6PC |
Abbre | G6PC |
Synonyms | AW107337, G-6-Pase, G6PC, G6PT, G6Pase, G6Pase-alpha, GSD1, GSD1a, Glucose-6-phosphatase, Glucose-6-phosphatase alpha, MGC163350, MGC93613, RP23-281C18.19, g6pc |
Swissprot | |
Cellular Localization | Endoplasmic reticulum membrane. |
Concentration | 1.44 mg/mL |
Buffer | Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol. |
Purification Method | Antigen affinity purification |
Research Areas | Cancer, Cell Biology, Metabolism |
Conjugation | Unconjugated |
Storage | Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles. |
Shipping | The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended. |
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. |
Other Clones
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Other Formats
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Unconjugated
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