Product Datasheet  
HADHSC Antibody  
Catalog Number: 48110  
Technical:tech@swbio.com  
Information:info@swbio.com  
Description  
  • host_species：  
  • Mouse
  • Amount：  
  • 100μgμg
  • Swiss-Prot No.：  
  • Swiss-Prot#:Q16836
  • Form of Antibody：  
  • 1*TBS (pH7.4), 0.5%BSA, 40%Glycerol. Preservative: 0.05% Sodium Azide.
  • Storage：  
  • Store at -20˚C
  • Immunogen：  
  • peptide
  • reactivity：  
  • Hu, Ms, zebrafish
  • appl_detail：  
  • WB: 1:1,000-1:2,000

    ICC: 1:500

  • other_names：  
  • 3 hydroxyacyl Coenzyme A dehydrogenase antibody
    HAD antibody
    HADH antibody
    HADH1 antibody
    HADHSC antibody
    HADHSC, formerly antibody
    HADSC, formerly antibody
    HCDH antibody
    HCDH_HUMAN antibody
    HHF4 antibody
    Hydroxyacyl CoA dehydrogenase antibody
    Hydroxyacyl-coenzyme A dehydrogenase antibody
    hydroxyacyl-coenzyme A dehydrogenase, mitochondrial antibody
    L 3 hydroxyacyl Coenzyme A dehydrogenase short chain antibody
    M SCHAD antibody
    Medium and short chain L 3 hydroxyacyl coenzyme A dehydrogenase antibody
    Medium and short-chain L-3-hydroxyacyl-coenzyme A dehydrogenase antibody
    MGC8392 antibody
    mitochondrial antibody
    MSCHAD antibody
    OTTHUMP00000162626 antibody
    OTTHUMP00000219688 antibody
    SCHAD antibody
    SCHAD, formerly antibody
    Short chain 3 hydroxyacyl CoA dehydrogenase mitochondrial antibody
    short chain 3-hydroxyacyl-coa dehydrogenase antibody
    Short-chain 3-hydroxyacyl-CoA dehydrogenase antibody
  • Purification：  
  • ProA affinity purified
  • Specificity：  
  • Applications：  
  • WB, ICC, IHC
  • Background：  
  • Hydroxyacyl-Coenzyme A dehydrogenase also known as HADH is an enzyme which in humans is encoded by the HADH gene. 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. A deficiency is associated with 3-hydroxyacyl-coenzyme A dehydrogenase deficiency.



 
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