KPYR Polyclonal Antibody, 20ul Protein Modification The encoded protein has been

The encoded protein has been found in brain

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

3-containing nucleosomes

Chromatin assembly factor I (CAF1) is a nuclear complex consisting of p50

This gene is a member of the Gal/GalNAc/GlcNAc (galactose/N-acetylgalactosamine/N-acetylglucosamine) 6-O-sulfotransferase (GST) family

KPYR Polyclonal Antibody, 20ul Protein Modification The encoded protein has beenThe 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.