PCBP1 Polyclonal Antibody, 20ul Enzymes Mutations in this gene cause

Mutations in this gene cause abnormal migration of neurons during development and disrupt the layering of the cortex

Mutations in this gene are associated with Goldberg-Shprintzen megacolon syndrome

The muscle acetylcholine receptor is composed of five subunits: two alpha subunits and one beta

Peroxisomal multifunctional enzyme type 2 encoded by HSD17B4 is a bifunctional enzyme that is involved in the peroxisomal beta-oxidation pathway for fatty acids

This protein associates with transcription complexes and with acetylated chromatin during mitosis

PCBP1 Polyclonal Antibody, 20ul Enzymes Mutations in this gene causeThis intronless gene is thought to have been generated by retrotransposition of a fully processed PCBP 2 mRNA. This gene and PCBP 2 have paralogues (PCBP3 and PCBP4) which are thought to have arisen as a result of duplication events of entire genes. The protein encoded by this gene appears to be multifunctional. It along with PCBP 2 and hnRNPK corresponds to the major cellular poly(rC) binding protein. It contains three K homologous (KH) domains which