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Last updated: 2016/12/11
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ABHD5 polyclonal antibody

  • Catalog # : PAB12500
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  • Specification
  • Product Description:
  • Rabbit polyclonal antibody raised against synthetic peptide of ABHD5.
  • Immunogen:
  • A synthetic peptide corresponding to amino acids 200-300 of human ABHD5.
  • Host:
  • Rabbit
  • Reactivity:
  • Human
  • Form:
  • Liquid
  • Quality Control Testing:
  • Antibody Reactive Against Synthetic Peptide.
  • Recommend Usage:
  • Western Blot (0.5 ug/mL)
    The optimal working dilution should be determined by the end user.
  • Storage Buffer:
  • In Tris-glycine, 150 mM NaCl (0.05% sodium azide)
  • Storage Instruction:
  • Store at 4°C for short term. For long term storage 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 (Cell lysate)
  • Western Blot (Cell lysate)
  • Western blot of ABHD5 in MCF-7 cell lysates using ABHD5 polyclonal antibody (Cat # PAB12500).
  • Western Blot (Transfected lysate)
  • Western Blot (Transfected lysate)
  • Western blot analysis of ABHD5 in ABHD5 overexpressed lysates using ABHD5 polyclonal antibody (Cat # PAB12500).
  • Application Image
  • Western Blot (Cell lysate)
  • Western Blot (Cell lysate)
  • enlarge
  • Western Blot (Transfected lysate)
  • Western Blot (Transfected lysate)
  • enlarge
  • Gene Information
  • Gene Name:
  • ABHD5
  • Gene Alias:
  • CDS,CGI58,IECN2,MGC8731,NCIE2
  • Gene Description:
  • abhydrolase domain containing 5
  • Gene Summary:
  • The protein encoded by this gene belongs to a large family of proteins defined by an alpha/beta hydrolase fold, and contains three sequence motifs that correspond to a catalytic triad found in the esterase/lipase/thioesterase subfamily. It differs from other members of this subfamily in that its putative catalytic triad contains an asparagine instead of the serine residue. Mutations in this gene have been associated with Chanarin-Dorfman syndrome, a triglyceride storage disease with impaired long-chain fatty acid oxidation. [provided by RefSeq
  • Other Designations:
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