TTR mouse Monoclonal Antibody(4E4), 20ul Plates & Dishes Mutations in this gene cause

Mutations in this gene cause cardiofaciocutaneous syndrome (CFC syndrome)

Multiple transcript variants encoding different isoforms have been found for CHAT

It plays an essential role in T-cell interactions and also in T-cell/B-cell interaction during early lymphoid development

This receptor specifically binds to IL17B and IL17E

TTR mouse Monoclonal Antibody(4E4), 20ul Plates & Dishes Mutations in this gene causeThis gene encodes transthyretin, one of the three prealbumins including alpha 1 antitrypsin, transthyretin and orosomucoid. Transthyretin is a carrier protein it transports thyroid hormones in the plasma and cerebrospinal fluid, and also transports retinol (vitamin A) in the plasma. The protein consists of a tetramer of identical subunits. More than 80 different mutations in this gene have been reported most mutations are related to amyloid