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G6PC antibody

The Rabbit Polyclonal anti-G6PC antibody has been validated for ELISA and IHC. It is suitable to detect G6PC in samples from Human, Mouse and Rat.
Catalog No. ABIN7245446

Quick Overview for G6PC antibody (ABIN7245446)

Target

See all G6PC Antibodies
G6PC (Glucose 6-Phosphatase, Catalytic (G6PC))

Reactivity

  • 45
  • 22
  • 22
  • 16
  • 14
  • 13
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 46
  • 3
Rabbit

Clonality

  • 46
  • 3
Polyclonal

Conjugate

  • 17
  • 5
  • 4
  • 4
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This G6PC antibody is un-conjugated

Application

  • 37
  • 20
  • 18
  • 11
  • 11
  • 6
  • 6
  • 4
  • 1
ELISA, Immunohistochemistry (IHC)
  • Characteristics

    Polyclonal Antibody

    Purification

    Antigen affinity purification

    Immunogen

    Synthetic peptide of human G6PC

    Isotype

    IgG
  • Application Notes

    IHC 1:50-1:300, ELISA 1:5000-1:10000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1.44 mg/mL

    Buffer

    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    G6PC (Glucose 6-Phosphatase, Catalytic (G6PC))

    Alternative Name

    G6PC

    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.

    UniProt

    P35575

    Pathways

    Carbohydrate Homeostasis, Cellular Glucan Metabolic Process
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