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Glycogen Synthase 2 Protein (Myc-DYKDDDDK Tag)

GYS2 Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2722378
  • Antigène Voir toutes Glycogen Synthase 2 (GYS2) Protéines
    Glycogen Synthase 2 (GYS2) (Glycogen Synthase 2, Liver (GYS2))
    Type de proteíne
    Recombinant
    Origine
    • 4
    • 1
    • 1
    • 1
    Humain
    Source
    • 2
    • 2
    • 2
    • 1
    HEK-293 Cells
    Purification/Conjugué
    Cette Glycogen Synthase 2 protéine est marqué à la Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human GYS2 protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Pureté
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product GYS2 Protéine
  • Indications d'application
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Commentaires

    The tag is located at the C-terminal.

    Restrictions
    For Research Use only
  • Concentration
    50 μg/mL
    Buffer
    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
    Stock
    -80 °C
    Stockage commentaire
    Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
  • Antigène
    Glycogen Synthase 2 (GYS2) (Glycogen Synthase 2, Liver (GYS2))
    Autre désignation
    Gys2 (GYS2 Produits)
    Synonymes
    cb765 Protein, zgc:112057 Protein, BC021322 Protein, LGS Protein, GLYSN Protein, glycogen synthase 2 Protein, gys2 Protein, Gys2 Protein, GYS2 Protein
    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.
    Poids moléculaire
    80.8 kDa
    NCBI Accession
    NP_068776
    Pathways
    AMPK Signaling, Cellular Glucan Metabolic Process
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