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WB analysis of NIH-3T3 lysate using GTX89147 ABHD5 antibody, Internal. Dilution : 0.2microg/ml Loading : 35microg protein in RIPA buffer
WB analysis of NIH-3T3 lysate using GTX89147 ABHD5 antibody, Internal. Dilution : 0.2microg/ml Loading : 35microg protein in RIPA buffer
WB analysis of NIH-3T3 lysate using GTX89147 ABHD5 antibody, Internal. Dilution : 0.2microg/ml Loading : 35microg protein in RIPA buffer

ABHD5 antibody, Internal

GTX89147
GeneTex
ApplicationsWestern Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityHuman, Mouse
TargetABHD5
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Overview

  • Supplier
    GeneTex
  • Product Name
    ABHD5 antibody, Internal
  • Delivery Days Customer
    7
  • Antibody Specificity
    This antibody is not expected to cross-react with ABHD4.
  • Application Supplier Note
    WB: 0.2-0.6microg/ml. IHC-P: 3.75microg/ml. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    0.50 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID51099
  • Target name
    ABHD5
  • Target description
    abhydrolase domain containing 5, lysophosphatidic acid acyltransferase
  • Target synonyms
    1-acylglycerol-3-phosphate O-acyltransferase ABHD5; abhydrolase domain-containing protein 5; CGI58; IECN2; lipid droplet-binding protein CGI-58; NCIE2; truncated abhydrolase domain-containing protein 5
  • Host
    Goat
  • Isotype
    IgG
  • Protein IDQ8WTS1
  • Protein Name
    1-acylglycerol-3-phosphate O-acyltransferase ABHD5
  • Scientific Description
    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, Jul 2008]
  • Reactivity
    Human, Mouse
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203