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KPYR Polyclonal Antibody, 20ul Protein Modification It is a member of

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KPYR Polyclonal Antibody, 20ul Protein Modification It is a member ofThe 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.

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Description

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

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

The RAMP1 protein is involved in the terminal glycosylation

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

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

KPYR Polyclonal Antibody, 20ul Protein Modification It is a member ofThe 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.

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