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Medium-Chain Specific Acyl-CoA Dehydrogenase, Mitochondrial anticorps

Reactivité: Humain, Souris, Rat IF Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN5965186
  • Antigène
    Medium-Chain Specific Acyl-CoA Dehydrogenase, Mitochondrial
    Reactivité
    • 52
    • 19
    • 16
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Humain, Souris, Rat
    Hôte
    • 46
    • 4
    • 2
    Lapin
    Clonalité
    • 48
    • 3
    Polyclonal
    Conjugué
    • 26
    • 4
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Inconjugué
    Application
    • 24
    • 15
    • 14
    • 13
    • 11
    • 10
    • 8
    • 4
    • 3
    • 3
    • 1
    • 1
    • 1
    Immunofluorescence (IF)
    Purification
    Affinity purification
    Immunogène
    Recombinant fusion protein of human ACADM (NP_000007.1).
    Isotype
    IgG
  • Indications d'application
    IF 1:50-1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/mL
    Buffer
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    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
    Medium-Chain Specific Acyl-CoA Dehydrogenase, Mitochondrial
    Autre désignation
    ACADM
    Synonymes
    anticorps ACAD1, anticorps MCAD, anticorps MCADH, anticorps AU018656, anticorps acyl-CoA dehydrogenase medium chain, anticorps acyl-Coenzyme A dehydrogenase, medium chain, anticorps acyl-CoA dehydrogenase, C-4 to C-12 straight chain, anticorps ACADM, anticorps Acadm
    Sujet
    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.
    Poids moléculaire

    Observed_MW: 47kDa

    Calculated_MW: 46kDa/47kDa

    ID gène
    34
    UniProt
    P11310
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