S12A3 Rabbit Polyclonal Antibody, 100ul Peptide Synthesis where CENP-B is localized

where CENP-B is localized

Mutations in this gene may be associated with iron overload in human patients

This gene has been implicated in numerous human cancers and may act as a metastasis suppressor gene

tissue specificity:Preferentially detected in breast carcinoma tissue and mammary gland

S12A3 Rabbit Polyclonal Antibody, 100ul Peptide Synthesis where CENP-B is localizedThis gene encodes a renal thiazide sensitive sodium chloride cotransporter that is important for electrolyte homeostasis. This cotransporter mediates sodium and chloride reabsorption in the distal convoluted tubule. Mutations in this gene cause Gitelman syndrome a disease similar to Bartter's syndrome that is characterized by hypokalemic alkalosis combined with hypomagnesemia low urinary calcium and increased renin activity associated with normal