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

Mutations in this gene cause cardiofaciocutaneous syndrome (CFC syndrome)

this protein is considered a member of the cytochrome P450 superfamily on the basis of sequence similarity rather than functional similarity

The binding of this protein to IL3 depends on the beta subunit

This protein also functions as a transporter in the blood-brain barrier

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