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SLC27A2 antibody [HL2232]

GTX638277
GeneTex
ApplicationsWestern Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityHuman, Mouse, Rat
TargetSLC27A2
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Overview

  • Supplier
    GeneTex
  • Product Name
    SLC27A2 antibody [HL2232]
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1:500-1:3000. *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
    Monoclonal
  • Clone ID
    HL2232
  • Concentration
    1 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID11001
  • Target name
    SLC27A2
  • Target description
    solute carrier family 27 member 2
  • Target synonyms
    ACSVL1; arachidonate--CoA ligase; FACVL1; FATP2; FATP-2; fatty acid transport protein 2; fatty-acid-coenzyme A ligase, very long-chain 1; hFACVL1; HsT17226; long-chain-fatty-acid--CoA ligase; phytanate--CoA ligase; solute carrier family 27 (fatty acid transporter), member 2; THCA-CoA ligase; very long-chain acyl-CoA synthetase; very long-chain fatty-acid-coenzyme A ligase 1; very long-chain-fatty-acid-CoA ligase; VLACS; VLCS
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDO14975
  • Protein Name
    Very long-chain acyl-CoA synthetase
  • Scientific Description
    The protein encoded by this gene is an isozyme of long-chain fatty-acid-coenzyme A ligase family. Although differing in substrate specificity, subcellular localization, and tissue distribution, all isozymes of this family convert free long-chain fatty acids into fatty acyl-CoA esters, and thereby play a key role in lipid biosynthesis and fatty acid degradation. This isozyme activates long-chain, branched-chain and very-long-chain fatty acids containing 22 or more carbons to their CoA derivatives. It is expressed primarily in liver and kidney, and is present in both endoplasmic reticulum and peroxisomes, but not in mitochondria. Its decreased peroxisomal enzyme activity is in part responsible for the biochemical pathology in X-linked adrenoleukodystrophy. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2009]
  • Reactivity
    Human, Mouse, Rat
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203