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Glycogen Synthase 2 anticorps

GYS2 Reactivité: Humain, Souris, Rat ELISA, IHC Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7237113
  • Antigène Voir toutes Glycogen Synthase 2 (GYS2) Anticorps
    Glycogen Synthase 2 (GYS2) (Glycogen Synthase 2, Liver (GYS2))
    Reactivité
    • 18
    • 17
    • 14
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Humain, Souris, Rat
    Hôte
    • 27
    • 2
    Lapin
    Clonalité
    • 27
    • 2
    Polyclonal
    Conjugué
    • 8
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp Glycogen Synthase 2 est non-conjugé
    Application
    • 22
    • 13
    • 13
    • 6
    • 3
    • 3
    ELISA, Immunohistochemistry (IHC)
    Attributs du produit
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogène
    Recombinant protein of human GYS2
    Isotype
    IgG
  • Indications d'application
    IHC 1:100-1:300
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.3 mg/mL
    Buffer
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    Agent conservateur
    Sodium azide
    Précaution d'utilisation
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Stock
    -20 °C
    Stockage commentaire
    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène
    Glycogen Synthase 2 (GYS2) (Glycogen Synthase 2, Liver (GYS2))
    Autre désignation
    GYS2 (GYS2 Produits)
    Synonymes
    anticorps cb765, anticorps zgc:112057, anticorps BC021322, anticorps LGS, anticorps GLYSN, anticorps glycogen synthase 2, anticorps gys2, anticorps Gys2, anticorps GYS2
    Sujet
    The protein encoded by this gene, liver glycogen synthase, catalyzes the rate-limiting step in the synthesis of glycogen - the transfer of a glucose molecule from UDP-glucose to a terminal branch of the glycogen molecule. Mutations in this gene cause glycogen storage disease type 0 (GSD-0) - a rare type of early childhood fasting hypoglycemia with decreased liver glycogen content.
    UniProt
    P54840
    Pathways
    AMPK Signaling, Cellular Glucan Metabolic Process
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