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ACSL4 Polyclonal Antibody Store at -20°C

SKU: E-AB-14661-200

  • $ 55995
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ACSL4 Polyclonal Antibody Store at -20°C

 

SKU # E-AB-14661
Reactivity Human,  Mouse,  Rat
Host Rabbit
Applications WB,  IHC

 

Product Details

Isotype IgG
Host Rabbit
Reactivity Human,  Mouse,  Rat
Applications WB,  IHC
Clonality Polyclonal
Immunogen Recombinant protein of human ACSL4
Abbre ACSL4
Synonyms ACS 4,  ACS4,  ACSL 4,  ACSL4,  Acsl4,  Acyl CoA synthetase long chain family member 4,  FACL 4,  FACL4,  Fatty acid Coenzyme A ligase,  LACS 4,  LACS4,  Lignoceroyl CoA synthase,  Long chain 4,  acyl CoA synthetase 4,  fatty acid Coenzyme A ligase long-chain 4,  long chain acyl CoA s
Swissprot
Calculated MW 79 kDa
Cellular Localization Mitochondrion outer membrane. Peroxisome membrane. Microsome membrane. Endoplasmic reticulum membrane.
Concentration 0.2 mg/mL
Buffer Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol.
Purification Method Affinity purification
Research Areas Cancer,  Metabolism,  Signal Transduction
Conjugation Unconjugated
Storage Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.
Shipping The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended.

 

Related Reagents

Applications Recommended Dilution
WB 1:1000-1:5000
IHC 1:50-1:200

 

Background

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.