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GCDH Antikörper

GCDH Reaktivität: Human, Maus IHC, ELISA Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN7004050
  • Target Alle GCDH Antikörper anzeigen
    GCDH (Glutaryl-CoA Dehydrogenase (GCDH))
    Reaktivität
    • 53
    • 9
    • 8
    • 6
    • 5
    • 4
    • 4
    • 4
    • 4
    • 4
    • 3
    • 1
    • 1
    Human, Maus
    Wirt
    • 51
    • 3
    Kaninchen
    Klonalität
    • 54
    Polyklonal
    Konjugat
    • 26
    • 5
    • 4
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser GCDH Antikörper ist unkonjugiert
    Applikation
    • 50
    • 22
    • 21
    • 13
    • 13
    • 8
    • 5
    • 4
    • 3
    • 3
    • 1
    Immunohistochemistry (IHC), ELISA
    Produktmerkmale
    Polyclonal Antibody
    Aufreinigung
    Antigen affinity purification
    Immunogen
    Fusion protein of human GCDH
    Isotyp
    IgG
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  • Applikationshinweise
    IHC 1:30-1:150, ELISA 1:5000-1:10000
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    1.02 mg/mL
    Buffer
    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    GCDH (Glutaryl-CoA Dehydrogenase (GCDH))
    Andere Bezeichnung
    GCDH (GCDH Produkte)
    Synonyme
    ACAD5 antikoerper, GCD antikoerper, zgc:56505 antikoerper, zgc:77704 antikoerper, 9030411L18 antikoerper, AI266902 antikoerper, D17825 antikoerper, glutaryl-CoA dehydrogenase antikoerper, glutaryl-CoA dehydrogenase a antikoerper, glutaryl-Coenzyme A dehydrogenase antikoerper, GCDH antikoerper, Gcdh antikoerper, gcdha antikoerper
    Hintergrund
    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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