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WB analysis of human heart lysate using GTX13677 ACADM antibody, C-term. Dilution : 0.05microg/ml Loading : 35microg protein in RIPA buffer
WB analysis of human heart lysate using GTX13677 ACADM antibody, C-term. Dilution : 0.05microg/ml Loading : 35microg protein in RIPA buffer
WB analysis of human heart lysate using GTX13677 ACADM antibody, C-term. Dilution : 0.05microg/ml Loading : 35microg protein in RIPA buffer

ACADM antibody, C-term

GTX13677
GeneTex
ApplicationsWestern Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityHuman
TargetACADM
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Overview

  • Supplier
    GeneTex
  • Product Name
    ACADM antibody, C-term
  • Delivery Days Customer
    9
  • Antibody Specificity
    This antibody is expected to recognise both reported isoforms (NP_000007.1; NP_001120800.1).
  • Application Supplier Note
    WB: 0.01-0.1microg/ml. IHC-P: 3-5microg/ml. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    0.50 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID34
  • Target name
    ACADM
  • Target description
    acyl-CoA dehydrogenase medium chain
  • Target synonyms
    ACAD1; acyl-CoA dehydrogenase, C-4 to C-12 straight chain; acyl-Coenzyme A dehydrogenase, C-4 to C-12 straight chain; MCAD; MCADH; medium-chain acyl-CoA dehydrogenase; medium-chain specific acyl-CoA dehydrogenase, mitochondrial; testicular tissue protein Li 7
  • Host
    Goat
  • Isotype
    IgG
  • Protein IDP11310
  • Protein Name
    Medium-chain specific acyl-CoA dehydrogenase, mitochondrial
  • Scientific Description
    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]
  • Reactivity
    Human
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203