ACSL4/FACL4 Antibody

ACSL4 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 [taken from NCBI Entrez Gene (Gene ID: 2182)].
ACSL4
acyl-CoA synthetase long-chain family member 4
Long-chain-fatty-acid--CoA ligase 4
:  ACS4 acyl-CoA synthetase 4 FACL4 fatty-acid-Coenzyme A ligase, long-chain 4 LACS 4 LACS4 lignoceroyl-CoA synthase long-chain acyl-CoA synthetase 4 long-chain fatty-acid-Coenzyme A ligase 4 mental retardation, X-linked 63 mental retardation, X-linked 68 MRX63 MRX68 More... Less...
Product
Specifications
Ordering Information
Human
WB, IP
between 250 and 300
100
$339
$229
$99