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Medium-Chain Specific Acyl-CoA Dehydrogenase, Mitochondrial anticorps

Reactivité: Humain WB, IHC, IF Hôte: Lapin Monoclonal unconjugated
N° du produit ABIN7101707
  • Antigène
    Medium-Chain Specific Acyl-CoA Dehydrogenase, Mitochondrial
    Reactivité
    • 53
    • 19
    • 16
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Humain
    Hôte
    • 47
    • 4
    • 2
    Lapin
    Clonalité
    • 48
    • 4
    Monoclonal
    Conjugué
    • 27
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Inconjugué
    Application
    • 25
    • 15
    • 14
    • 13
    • 12
    • 11
    • 8
    • 4
    • 4
    • 3
    • 3
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
     Réactivité croisée
    Humain, Souris, Rat
    Attributs du produit
    Monoclonal Antibodies
    Purification
    Affinity purification
    Immunogène
    A synthesized peptide derived from human ACADM
    Isotype
    IgG
  • Indications d'application
    WB,1:500 - 1:2000,IHC,1:50 - 1:200,IF,1:50 - 1:200
    Restrictions
    For Research Use only
  • Buffer
    PBS with 0.02 % sodium azide,0.05 % BSA,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. [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
    Poids moléculaire
    46 kDa
    ID gène
    34
    UniProt
    P11310
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