KLF14 Polyclonal Antibody, 50ul Antibody Humanization Two transcript variants encoding different

Two transcript variants encoding different isoforms have been found for CA2

Mutations in this gene result in a variety of hereditary red blood cell disorders| including elliptocytosis type 2| pyropoikilocytosis| and spherocytic hemolytic anemia

impairs kinetochore assembly and chromosome alignment

The encoded protein directly interacts with a GTPase activating protein that functions downstream of the small G protein Ral

Tumor necrosis factor receptor superfamily member 3 plays a role in signalling during the development of lymphoid and other organs

KLF14 Polyclonal Antibody, 50ul Antibody Humanization Two transcript variants encoding differentThis intronless gene encodes a member of the Kruppel like family of transcription factors. The encoded protein functions as a transcriptional co repressor, and is induced by transforming growth factor beta (TGF beta) to repress TGF beta receptor II gene expression. This gene exhibits imprinted expression from the maternal allele in embryonic and extra embryonic tissues.