Bmx Polyclonal Antibody, 100ul[BT-AP00941] Cell Function Analysis It has been found to

It has been found to be constituitively associated with the prolactin receptor and is required for responses to gamma interferon

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

The protein encoded by this gene is a member of the FPS/FES family of non-transmembrane receptor tyrosine kinases

an acid and a nucleophile

Bmx Polyclonal Antibody, 100ul[BT-AP00941] Cell Function Analysis It has been found toBMX encodes a non receptor tyrosine kinase belonging to the Tec kinase family. The protein (BMX non receptor tyrosine kinase)contains a PH like domain, which mediates membrane targeting by binding to phosphatidylinositol 3,4,5 triphosphate (PIP3), and a SH2 domain that binds to tyrosine phosphorylated proteins and functions in signal transduction. The protein is implicated in several signal transduction pathways including the Stat pathway, and