TTR mouse Monoclonal Antibody(4A12), 100ul DNA Libraries Synthesis A splice-site mutation in this

A splice-site mutation in this gene has been associated with a novel progressive myoclonic epilepsy disease with similar symptoms to MERRF syndrome

is ubiquitously expressed and localized in the cytoplasm

This subunit is present in 4-5 copies per dynactin molecule

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A pseudogene corresponding to MRPL32 is found on chromosome Xp

TTR mouse Monoclonal Antibody(4A12), 100ul DNA Libraries Synthesis A splice-site mutation in thisThis 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