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Medium-Chain Specific Acyl-CoA Dehydrogenase, Mitochondrial Antikörper

Reaktivität: Human WB, IHC, IF Wirt: Kaninchen Monoclonal unconjugated
Produktnummer ABIN7101707
  • Target
    Medium-Chain Specific Acyl-CoA Dehydrogenase, Mitochondrial
    Reaktivität
    • 52
    • 19
    • 16
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Human
    Wirt
    • 46
    • 4
    • 2
    Kaninchen
    Klonalität
    • 48
    • 3
    Monoklonal
    Konjugat
    • 26
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Unkonjugiert
    Applikation
    • 24
    • 15
    • 14
    • 13
    • 11
    • 10
    • 8
    • 4
    • 3
    • 3
    • 2
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
    Kreuzreaktivität
    Human, Maus, Ratte
    Produktmerkmale
    Monoclonal Antibodies
    Aufreinigung
    Affinity purification
    Immunogen
    A synthesized peptide derived from human ACADM
    Isotyp
    IgG
  • Applikationshinweise
    WB,1:500 - 1:2000,IHC,1:50 - 1:200,IF,1:50 - 1:200
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Buffer
    PBS with 0.02 % sodium azide,0.05 % BSA,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. [provided by RefSeq, Jul 2008],ACAD1, MCAD, MCADH,Cancer,Cardiovascular,Endocrine & Metabolism,Lipid Metabolism,Lipids,Lipids_Fatty Acids,Mitochondrial metabolism,Mitochondrial metabolism_Mitochondrial markers,Signal Transduction,ACADM
    Molekulargewicht
    46 kDa
    Gen-ID
    34
    UniProt
    P11310
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