LPCAT2 Polyclonal Antibody, 50ul Variant Libraries Mutations in this gene are

Mutations in this gene are a cause of spastic ataxia 2| autosomal recessive

a Caenorhabditis elegans gene involved in axon guidance

and belongs to the type I cytokine receptor family

This subunit may associate with a beta 1 or beta 4 subunit to form an integrin that interacts with extracellular matrix proteins including members of the laminin family

LPCAT2 Polyclonal Antibody, 50ul Variant Libraries Mutations in this gene areLPCAT2 (lysophosphatidylcholine acyltransferase 2) encodes a member of the lysophospholipid acyltransferase family. The encoded enzyme may function in two ways: to catalyze the biosynthesis of platelet activating factor (1 O alkyl 2 acetyl sn glycero 3 phosphocholine) from 1 O alkyl sn glycero 3 phosphocholine, and to catalyze the synthesis of glycerophospholipid precursors from arachidonyl CoA and lysophosphatidylcholine. The encoded protein may