Anti-FATP2/SLC27A2 Antibody Picoband®

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.

SLC27A2; ACSVL1; FACVL1; FATP2; VLACS; Very long-chain acyl-CoA synthetase; VLACS; VLCS; EC 6.2.1.-; Arachidonate--CoA ligase; EC 6.2.1.15; Fatty acid transport protein 2; FATP-2; Fatty-acid-coenzyme A ligase, very long-chain 1; Long-chain-fatty-acid--CoA ligase; EC 6.2.1.3; Phytanate--CoA ligase; EC 6.2.1.24; Solute carrier family 27 member 2; THCA-CoA ligase; EC 6.2.1.7; Very long-chain-fatty-acid-CoA ligase

E.coli-derived human FATP2/SLC27A2 recombinant protein (Position: F27-D608) . Human FATP2/SLC27A2 shares 83.3% and 83.1% amino acid (aa) sequence identity with mouse and rat FATP2/SLC27A2, respectively.

At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month. It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.