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Glucose 6-Phosphatase, Catalytic (G6PC) (N-Term) Peptide

G6PC Reactivity: Human Host: Synthetic BP, WB, IHC
Catalog No. ABIN977184

Quick Overview for Glucose 6-Phosphatase, Catalytic (G6PC) (N-Term) Peptide (ABIN977184)

Target

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

Origin

Human

Source

  • 3
Synthetic

Application

Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
  • Protein Region

    N-Term

    Characteristics

    This is a synthetic peptide designed for use in combination with anti-G6PC antibody (Catalog #: ARP44224_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.

    Purification

    Purified
  • Application Notes

    Each Investigator should determine their own optimal working dilution for specific applications.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.

    Concentration

    1 mg/mL

    Buffer

    Final peptide concentration is 1 mg/mL in PBS.

    Handling Advice

    Avoid repeated freeze-thaw cycles.

    Storage

    -20 °C

    Storage Comment

    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Target

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

    Background

    G6PC hydrolyzes glucose-6-phosphate to glucose in the endoplasmic reticulum.It forms with the glucose-6-phosphate transporter (SLC37A4/G6PT) the complex responsible for glucose production through glycogenolysis and gluconeogenesis. Hence, it is the key enzyme in homeostatic regulation of blood glucose levels.Glucose-6-phosphatase is an integral membrane protein of the endoplasmic reticulum that catalyzes the hydrolysis of D-glucose 6-phosphate to D-glucose and orthophosphate. It is a key enzyme in glucose homeostasis, functioning in gluconeogenesis and glycogenolysis. Defects in the enzyme cause glycogen storage disease type I (von Gierke disease). Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.

    Alias Symbols: G6PT, GSD1a, MGC163350, GSD1, G6PC1

    Protein Interaction Partner: FOXO1

    Protein Size: 357

    Molecular Weight

    40 kDa

    Gene ID

    2538

    NCBI Accession

    NM_000151, NP_000142

    UniProt

    P35575
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