S12A3 Rabbit Polyclonal Antibody, 20ul Oligo Pool Mutations in this gene can

Mutations in this gene can cause radio-ulnar synostosis with amegakaryocytic thrombocytopenia

These activities suggest that this receptor may be of physiological importance and that a natural agonist for the receptor may exist

and are involved in long-term potentiation

forkhead box protein B2

but share a C-terminal leucine zipper for dimerization and DNA binding

S12A3 Rabbit Polyclonal Antibody, 20ul Oligo Pool Mutations in this gene canThis 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