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GCDH anticorps

GCDH Reactivité: Humain, Souris IHC, ELISA Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7004050
  • Antigène Voir toutes GCDH Anticorps
    GCDH (Glutaryl-CoA Dehydrogenase (GCDH))
    Reactivité
    • 53
    • 9
    • 8
    • 6
    • 5
    • 4
    • 4
    • 4
    • 4
    • 4
    • 3
    • 1
    • 1
    Humain, Souris
    Hôte
    • 51
    • 3
    Lapin
    Clonalité
    • 54
    Polyclonal
    Conjugué
    • 26
    • 5
    • 4
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp GCDH est non-conjugé
    Application
    • 50
    • 22
    • 21
    • 13
    • 13
    • 8
    • 5
    • 4
    • 3
    • 3
    • 1
    Immunohistochemistry (IHC), ELISA
    Attributs du produit
    Polyclonal Antibody
    Purification
    Antigen affinity purification
    Immunogène
    Fusion protein of human GCDH
    Isotype
    IgG
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    Discover our top product GCDH Anticorps primaire
  • Indications d'application
    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
    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
    GCDH (Glutaryl-CoA Dehydrogenase (GCDH))
    Autre désignation
    GCDH (GCDH Produits)
    Synonymes
    anticorps ACAD5, anticorps GCD, anticorps zgc:56505, anticorps zgc:77704, anticorps 9030411L18, anticorps AI266902, anticorps D17825, anticorps glutaryl-CoA dehydrogenase, anticorps glutaryl-CoA dehydrogenase a, anticorps glutaryl-Coenzyme A dehydrogenase, anticorps GCDH, anticorps Gcdh, anticorps gcdha
    Sujet
    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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