ERMAP Polyclonal Antibody, 100ul Pipette Controller Although differing in substrate specificity|

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

and the alpha-fetoprotein and albumin genes are present in tandem in the same transcriptional orientation on chromosome 4

Defects in HSPB1 are a cause of Charcot-Marie-Tooth disease type 2F (CMT2F) and distal hereditary motor neuropathy (dHMN)

Defects in this gene may also contribute to autosomal dominant non-insulin-dependent diabetes mellitus type II (NIDDM)

ERMAP Polyclonal Antibody, 100ul Pipette Controller Although differing in substrate specificity|The protein encoded by this gene is a cell surface transmembrane protein that may act as an erythroid cell receptor, possibly as a mediator of cell adhesion. Polymorphisms in this gene are responsible for the Scianna Radin blood group system. Two transcript variants encoding the same protein have been found for this gene.