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HADH polyclonal antibody

  • Catalog # : PAB7412
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  • Specification
  • Product Description:
  • Goat polyclonal antibody raised against synthetic peptide of HADH.
  • Immunogen:
  • A synthetic peptide corresponding to human HADH.
  • Sequence:
  • C-YERGDASKEDID
  • Host:
  • Goat
  • Theoretical MW (kDa):
  • 34.3
  • Reactivity:
  • Human
  • Form:
  • Liquid
  • Purification:
  • Antigen affinity purification
  • Concentration:
  • 0.5 mg/mL
  • Quality Control Testing:
  • Antibody Reactive Against Synthetic Peptide.
  • Recommend Usage:
  • ELISA (1:64000)
    Western Blot (0.01-0.03 ug/mL)
    The optimal working dilution should be determined by the end user.
  • Storage Buffer:
  • In Tris saline, pH 7.3 (0.5% BSA, 0.02% sodium azide)
  • Storage Instruction:
  • Store at -20°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.
  • Publication Reference
  • Applications
  • Western Blot (Tissue lysate)
  • Western Blot (Tissue lysate)
  • HADH polyclonal antibody (Cat # PAB7412) (0.02 ug/mL) staining of human kidney lysate (35 ug protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.
  • Western Blot (Transfected lysate)
  • Western Blot (Transfected lysate)
  • 293 overexpressing HADH with C-terminal tag (DYKDDDDK) and probed with HADH polyclonal antibody (Cat # PAB7412) in the left panel.
  • ELISA
  • Application Image
  • Western Blot (Tissue lysate)
  • Western Blot (Tissue lysate)
  • enlarge
  • Western Blot (Transfected lysate)
  • Western Blot (Transfected lysate)
  • enlarge
  • 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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