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Last updated: 2016/12/4
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ABHD5 polyclonal antibody

  • Catalog # : PAB7219
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  • Specification
  • Product Description:
  • Goat polyclonal antibody raised against synthetic peptide of ABHD5.
  • Immunogen:
  • A synthetic peptide corresponding to internal region of human ABHD5.
  • Sequence:
  • C-FPERPDLADQDR
  • Host:
  • Goat
  • Theoretical MW (kDa):
  • 39.1
  • Reactivity:
  • Bovine, Human, Mouse
  • Specificity:
  • This antibody is not expected to cross-react with ABHD4.
  • Form:
  • Liquid
  • Purification:
  • Antigen affinity purification
  • Concentration:
  • 0.5 mg/mL
  • Recommend Usage:
  • ELISA (1:16000)
    Western Blot (0.2-0.6 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 (Cell lysate)
  • Western Blot (Cell lysate)
  • ABHD5 polyclonal antibody (Cat # PAB7219)(0.2 ug/mL) staining of NIH/3T3 lysate (35 ug protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.
  • ELISA
  • Application Image
  • Western Blot (Cell lysate)
  • Western Blot (Cell lysate)
  • enlarge
  • ELISA
  • 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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