S12A3 Rabbit Polyclonal Antibody, 20ul Oligo Pool and are involved in long-term

and are involved in long-term potentiation

bundling and anchoring microtubules to the centrosomes

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

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

forkhead box protein B2

S12A3 Rabbit Polyclonal Antibody, 20ul Oligo Pool and are involved in long-termThis 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