Bio-Connect
WB analysis of various sample lysates using GTX55529 BAAT antibody. Dilution : 1:2000 Loading : 25microg per lane
WB analysis of various sample lysates using GTX55529 BAAT antibody. Dilution : 1:2000 Loading : 25microg per lane
WB analysis of various sample lysates using GTX55529 BAAT antibody. Dilution : 1:2000 Loading : 25microg per lane

BAAT antibody

GTX55529
GeneTex
ApplicationsWestern Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityHuman, Mouse, Rat
TargetBAAT
Sign in to order and to see your custom pricing.
Large volume orders?
Order with a bulk request

Overview

  • Supplier
    GeneTex
  • Product Name
    BAAT antibody
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1:500 - 1:2000. IHC-P: 1:50 - 1:200. *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
  • Conjugate
    Unconjugated
  • Gene ID570
  • Target name
    BAAT
  • Target description
    bile acid-CoA:amino acid N-acyltransferase
  • Target synonyms
    BACAT; BACD1; BAT; bile acid CoA: amino acid N-acyltransferase (glycine N-choloyltransferase); bile acid Coenzyme A: amino acid N-acyltransferase (glycine N-choloyltransferase); bile acid-CoA thioesterase; bile acid-CoA:amino acid N-acyltransferase; choloyl-CoA hydrolase; HCHO; long-chain fatty-acyl-CoA hydrolase
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDQ14032
  • Protein Name
    Bile acid-CoA:amino acid N-acyltransferase
  • Scientific Description
    The protein encoded by this gene is a liver enzyme that catalyzes the transfer of C24 bile acids from the acyl-CoA thioester to either glycine or taurine, the second step in the formation of bile acid-amino acid conjugates. The bile acid conjugates then act as a detergent in the gastrointestinal tract, which enhances lipid and fat-soluble vitamin absorption. Defects in this gene are a cause of familial hypercholanemia (FHCA). Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]
  • Reactivity
    Human, Mouse, Rat
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203