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GCDH antibody

GCDH Reactivity: Human, Mouse IHC, ELISA Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7004050
  • Target See all GCDH Antibodies
    GCDH (Glutaryl-CoA Dehydrogenase (GCDH))
    Reactivity
    • 53
    • 9
    • 8
    • 6
    • 5
    • 4
    • 4
    • 4
    • 4
    • 4
    • 3
    • 1
    • 1
    Human, Mouse
    Host
    • 51
    • 3
    Rabbit
    Clonality
    • 54
    Polyclonal
    Conjugate
    • 26
    • 5
    • 4
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This GCDH antibody is un-conjugated
    Application
    • 50
    • 22
    • 21
    • 13
    • 13
    • 8
    • 5
    • 4
    • 3
    • 3
    • 1
    Immunohistochemistry (IHC), ELISA
    Characteristics
    Polyclonal Antibody
    Purification
    Antigen affinity purification
    Immunogen
    Fusion protein of human GCDH
    Isotype
    IgG
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    Discover our top product GCDH Primary Antibody
  • Application Notes
    IHC 1:30-1:150, ELISA 1:5000-1:10000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1.02 mg/mL
    Buffer
    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
    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
    GCDH (Glutaryl-CoA Dehydrogenase (GCDH))
    Alternative Name
    GCDH (GCDH Products)
    Synonyms
    ACAD5 antibody, GCD antibody, zgc:56505 antibody, zgc:77704 antibody, 9030411L18 antibody, AI266902 antibody, D17825 antibody, glutaryl-CoA dehydrogenase antibody, glutaryl-CoA dehydrogenase a antibody, glutaryl-Coenzyme A dehydrogenase antibody, GCDH antibody, Gcdh antibody, gcdha antibody
    Background
    The protein encoded by this gene belongs to the acyl-CoA dehydrogenase family. It catalyzes the oxidative decarboxylation of glutaryl-CoA to crotonyl-CoA and CO(2) in the degradative pathway of L-lysine, L-hydroxylysine, and L-tryptophan metabolism. It uses electron transfer flavoprotein as its electron acceptor. The enzyme exists in the mitochondrial matrix as a homotetramer of 45-kD subunits. Mutations in this gene result in the metabolic disorder glutaric aciduria type 1, which is also known as glutaric acidemia type I. Alternative splicing of this gene results in multiple transcript variants. A related pseudogene has been identified on chromosome 12.
    UniProt
    Q92947
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