TRXR1 Polyclonal Antibody, 100ul Peripheral Blood Separation Tube This protein is absent in

This protein is absent in patients with Duchenne and Becker types of muscular dystrophy

the gene also contains sequence encoding calcium-binding motifs found in all cadherins

Mutations in this gene have been associated with X-linked infantile spasm syndrome (ISSX)

100% tested for production line leakage

TRXR1 Polyclonal Antibody, 100ul Peripheral Blood Separation Tube This protein is absent inThis gene encodes a member of the family of pyridine nucleotide oxidoreductases. This protein reduces thioredoxins as well as other substrates, and plays a role in selenium metabolism and protection against oxidative stress. The functional enzyme is thought to be a homodimer which uses FAD as a cofactor. Each subunit contains a selenocysteine (Sec) residue which is required for Catalytic activity. The selenocysteine is encoded by the UGA codon that