LAT(Phospho-Tyr171) Rabbit Polyclonal Antibody, 100ul Liquid Handling Multiple transcript variants encoding different

Multiple transcript variants encoding different isoforms have been found for MYO9B

and other neoplasms

Mutations in this gene are associated with left ventricular noncompaction with congenital heart defects

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

RIMKLA contains one ATP-grasp domain and binds two manganese ions per subunit

LAT(Phospho-Tyr171) Rabbit Polyclonal Antibody, 100ul Liquid Handling Multiple transcript variants encoding differentThe protein encoded by this gene is phosphorylated by ZAP 70 Syk protein tyrosine kinases following activation of the T cell antigen receptor (TCR) signal transduction pathway. This transmembrane protein localizes to lipid rafts and acts as a docking site for SH2 domain containing proteins. Upon phosphorylation this protein recruits multiple adaptor proteins and downstream signaling molecules into multimolecular signaling complexes located near the