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phosphorylase, Glycogen, Liver (PYGL) (Middle Region) Peptide

PYGL Reactivité: Humain Hôte: Synthetic WB
N° du produit ABIN5518184
  • Antigène Tous les produits PYGL
    PYGL (phosphorylase, Glycogen, Liver (PYGL))
    Protein Region
    Middle Region
    Origine
    Humain
    Source
    • 2
    Synthetic
    Application
    Western Blotting (WB)
    Séquence
    SMATLGLAAY GYGIRYEYGI FNQKIRDGWQ VEEADDWLRY GNPWEKSRPE
  • Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    Stock
    -20 °C
    Stockage commentaire
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Antigène
    PYGL (phosphorylase, Glycogen, Liver (PYGL))
    Synonymes
    zgc:66314 Peptide, GSD6 Peptide, glycogen phosphorylase L Peptide, phosphorylase, glycogen, liver Peptide, phosphorylase, glycogen, liver S homeolog Peptide, liver glycogen phosphorylase Peptide, PYGL Peptide, pygl Peptide, pygl.S Peptide, Pygl Peptide
    Sujet
    This gene encodes a homodimeric protein that catalyses the cleavage of alpha-1,4-glucosidic bonds to release glucose-1-phosphate from liver glycogen stores. This protein switches from inactive phosphorylase B to active phosphorylase A by phosphorylation of serine residue 15. Activity of this enzyme is further regulated by multiple allosteric effectors and hormonal controls. Humans have three glycogen phosphorylase genes that encode distinct isozymes that are primarily expressed in liver, brain and muscle, respectively. The liver isozyme serves the glycemic demands of the body in general while the brain and muscle isozymes supply just those tissues. In glycogen storage disease type VI, also known as Hers disease, mutations in liver glycogen phosphorylase inhibit the conversion of glycogen to glucose and results in moderate hypoglycemia, mild ketosis, growth retardation and hepatomegaly. Alternative splicing results in multiple transcript variants encoding different isoforms.

    Alias Symbols: GSD6

    Protein Size: 167
    ID gène
    5836
    NCBI Accession
    NM_001163940, NP_001157412
    UniProt
    P06737
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