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HADH monoclonal antibody, clone 1A12BC8

  • Catalog # : MAB14068
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  • Specification
  • Product Description:
  • Mouse monoclonal antibody raised against human HADH.
  • Immunogen:
  • Human liver mitochondria.
  • Host:
  • Mouse
  • Reactivity:
  • Human
  • Form:
  • Liquid
  • Purification:
  • Purified
  • Isotype:
  • IgG1
  • Recommend Usage:
  • ELISA
    Immunocytochemistry (5 ug/mL)
    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
    Immunoprecipitation
    The optimal working dilution should be determined by the end user.
  • Storage Buffer:
  • In HEPES (0.02% sodium azide).
  • Storage Instruction:
  • Store at 4°C.
    Aliquot to avoid repeated freezing and thawing.
  • Note:
  • This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
  • Applications
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • Immunohistochemical staining (Formalin-fixed paraffin-embedded sections) of mitochondrial and metabolic enzymes in tissue sections of normal, aged human cerebellar tissue with HADH monoclonal antibody, clone 1A12BC8 (Cat # MAB14068).
  • Immunocytochemistry
  • Immunocytochemistry
  • Immunocytochemical staining of MRC5 fibroblasts with HADH monoclonal antibody, clone 1A12BC8 (Cat # MAB14068). Blue: nuclei.
  • Immunoprecipitation
  • ELISA
  • Application Image
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • enlarge
  • Immunoprecipitation
  • ELISA
  • Gene Information
  • Entrez GeneID:
  • 3033
  • Gene Name:
  • HADH
  • Gene Alias:
  • HAD,HADH1,HADHSC,HHF4,M/SCHAD,MGC8392,SCHAD
  • Gene Description:
  • hydroxyacyl-Coenzyme A dehydrogenase
  • Gene Summary:
  • This gene is a member of the 3-hydroxyacyl-CoA dehydrogenase gene family. The encoded protein functions in the mitochondrial matrix to catalyze the oxidation of straight-chain 3-hydroxyacyl-CoAs as part of the beta-oxidation pathway. Its enzymatic activity is highest with medium-chain-length fatty acids. Mutations in this gene cause one form of familial hyperinsulinemic hypoglycemia. The human genome contains a related pseudogene. [provided by RefSeq
  • Other Designations:
  • L-3-hydroxyacyl-Coenzyme A dehydrogenase,L-3-hydroxyacyl-Coenzyme A dehydrogenase, short chain
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