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Glycogen Synthase 2 antibody

GYS2 Reactivity: Human, Mouse, Rat ELISA, IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7237113
  • Target See all Glycogen Synthase 2 (GYS2) Antibodies
    Glycogen Synthase 2 (GYS2) (Glycogen Synthase 2, Liver (GYS2))
    Reactivity
    • 18
    • 17
    • 14
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Human, Mouse, Rat
    Host
    • 27
    • 2
    Rabbit
    Clonality
    • 27
    • 2
    Polyclonal
    Conjugate
    • 8
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This Glycogen Synthase 2 antibody is un-conjugated
    Application
    • 22
    • 13
    • 13
    • 6
    • 3
    • 3
    ELISA, Immunohistochemistry (IHC)
    Characteristics
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogen
    Recombinant protein of human GYS2
    Isotype
    IgG
  • Application Notes
    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
    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
    Glycogen Synthase 2 (GYS2) (Glycogen Synthase 2, Liver (GYS2))
    Alternative Name
    GYS2 (GYS2 Products)
    Synonyms
    cb765 antibody, zgc:112057 antibody, BC021322 antibody, LGS antibody, GLYSN antibody, glycogen synthase 2 antibody, gys2 antibody, Gys2 antibody, GYS2 antibody
    Background
    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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