KPYR Polyclonal Antibody, 20ul Protein Modification With 50 L per bottle

With 50 L per bottle

It is a member of the tetratricopeptide repeat family of proteins and acts as an inhibitor of the interferon-induced

Mutations in this gene have been associated with autosomal dominant high myopia (MYP24)

The encoded protein was thought to encode a protein precursor for two different proteins

The encoded protein may be involved in the regulation of antigen presentation

KPYR Polyclonal Antibody, 20ul Protein Modification With 50 L per bottleThe protein encoded by this gene is a pyruvate kinase that catalyzes the transphosphorylation of phohsphoenolpyruvate into pyruvate and ATP, which is the rate limiting step of glycolysis. Defects in this enzyme, due to gene mutations or genetic variations, are the common cause of chronic hereditary nonspherocytic hemolytic anemia (CNSHA or HNSHA). Multiple transcript variants encoding different isoforms have been found for this gene.