Bmx Polyclonal Antibody, 100ul[BT-AP00941] Cell Function Analysis Defects in HSPB1 are a

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

The protein encoded by FXR2 (FMR1 autosomal homolog 2) is a RNA binding protein containing two KH domains and one RCG box

MNDA is located within 2200 kb of FCER1A

Bmx Polyclonal Antibody, 100ul[BT-AP00941] Cell Function Analysis Defects in HSPB1 are aBMX 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