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Last updated: 2016/12/4
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ACSL4 polyclonal antibody

  • Catalog # : PAB6260
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  • Specification
  • Product Description:
  • Goat polyclonal antibody raised against synthetic peptide of ACSL4.
  • Immunogen:
  • A synthetic peptide corresponding to human ACSL4.
  • Sequence:
  • C-HYLKDIERMYGGK
  • Host:
  • Goat
  • Theoretical MW (kDa):
  • 74.4, 79.2
  • Reactivity:
  • Human
  • Specificity:
  • This antibody is expected to recognize both reported human isoforms, as represented by NP_004449 and NP_075266.
  • Form:
  • Liquid
  • Purification:
  • Antigen affinity purification
  • Concentration:
  • 0.5 mg/mL
  • Quality Control Testing:
  • Antibody Reactive Against Synthetic Peptide.
  • Recommend Usage:
  • ELISA (1:128000)
    Western blot (0.1-0.3 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)
  • ACSL4 polyclonal antibody (Cat # PAB6260) (0.1 ug/mL) staining of HepG2 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
  • Entrez GeneID:
  • 2182
  • Protein Accession#:
  • NP_004449;NP_075266
  • Gene Name:
  • ACSL4
  • Gene Alias:
  • ACS4,FACL4,LACS4,MRX63,MRX68
  • Gene Description:
  • acyl-CoA synthetase long-chain family member 4
  • Gene Summary:
  • The protein encoded by this gene is an isozyme of the 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 preferentially utilizes arachidonate as substrate. The absence of this enzyme may contribute to the mental retardation or Alport syndrome. Alternative splicing of this gene generates 2 transcript variants. [provided by RefSeq
  • Other Designations:
  • OTTHUMP00000023846,acyl-CoA synthetase 4,fatty-acid-Coenzyme A ligase, long-chain 4,lignoceroyl-CoA synthase,long-chain fatty-acid-Coenzyme A ligase 4
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