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Medium-Chain Specific Acyl-CoA Dehydrogenase, Mitochondrial Antikörper

Reaktivität: Human, Maus, Ratte IF Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN5965186
  • Target
    Medium-Chain Specific Acyl-CoA Dehydrogenase, Mitochondrial
    Reaktivität
    • 52
    • 19
    • 16
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Human, Maus, Ratte
    Wirt
    • 46
    • 4
    • 2
    Kaninchen
    Klonalität
    • 48
    • 3
    Polyklonal
    Konjugat
    • 26
    • 4
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Unkonjugiert
    Applikation
    • 24
    • 15
    • 14
    • 13
    • 11
    • 10
    • 8
    • 4
    • 3
    • 3
    • 1
    • 1
    • 1
    Immunofluorescence (IF)
    Aufreinigung
    Affinity purification
    Immunogen
    Recombinant fusion protein of human ACADM (NP_000007.1).
    Isotyp
    IgG
  • Applikationshinweise
    IF 1:50-1:200
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    1 mg/mL
    Buffer
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    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
    Medium-Chain Specific Acyl-CoA Dehydrogenase, Mitochondrial
    Andere Bezeichnung
    ACADM
    Synonyme
    ACAD1 antikoerper, MCAD antikoerper, MCADH antikoerper, AU018656 antikoerper, acyl-CoA dehydrogenase medium chain antikoerper, acyl-Coenzyme A dehydrogenase, medium chain antikoerper, acyl-CoA dehydrogenase, C-4 to C-12 straight chain antikoerper, ACADM antikoerper, Acadm antikoerper
    Hintergrund
    This gene encodes the medium-chain specific (C4 to C12 straight chain) acyl-Coenzyme A dehydrogenase. The homotetramer enzyme catalyzes the initial step of the mitochondrial fatty acid beta-oxidation pathway. Defects in this gene cause medium-chain acyl-CoA dehydrogenase deficiency, a disease characterized by hepatic dysfunction, fasting hypoglycemia, and encephalopathy, which can result in infantile death. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
    Molekulargewicht

    Observed_MW: 47kDa

    Calculated_MW: 46kDa/47kDa

    Gen-ID
    34
    UniProt
    P11310
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