E-AB-14661
ACSL4 Polyclonal Antibody
Size
£106.20
Was £118.00
- SKU:
- E-AB-14661
- Additional Names:
- 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
- Application:
- IHC, WB
- Concentration:
- 0.2 mg/ml
- Purification:
- Affinity Purified
- Storage Conditions:
- -20[o]C Avoid freeze/thaw cycles.
- Supplier:
- Elabscience
- Host:
- Rabbit
- Reactivities:
- Human, Mouse, Rat
- Buffer:
- Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol.
- Immunogen:
- Recombinant protein of human ACSL4
- Uniprot:
- O60488
- Synonyms:
- ACS4;acyl-CoA synthetase 4;arachidonate--CoA ligase;FACL4;fatty-acid-Coenzyme A ligase, long-chain 4;LACS4;lignoceroyl-CoA synthase;long-chain acyl-CoA synthetase 4;long-chain fatty-acid-Coenzyme A ligase 4;long-chain-fatty-acid--CoA ligase 4;MRX63;MRX68;XLID63
- Extra Details:
- 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.
- Shipping Conditions:
- Blue Ice