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G6PC Polyclonal Antibody Reactivity Rat

SKU: E-AB-52080-200

  • $ 55995


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G6PC Polyclonal Antibody Reactivity Rat

 

SKU # E-AB-52080
Reactivity Human, Mouse, Rat
Host Rabbit
Applications IHC

 

Product Details

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 2.04 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.

 

Related Reagents

Applications Recommended Dilution
IHC 1:70-1:350

 

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.