S12A3 Rabbit Polyclonal Antibody, 20ul Oligo Pool 2004 [PubMed 14744536])

2004 [PubMed 14744536])

bundling and anchoring microtubules to the centrosomes

forkhead box protein B2

YWHAH contains a 7 bp repeat sequence in its 5' UTR

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

S12A3 Rabbit Polyclonal Antibody, 20ul Oligo Pool 2004 [PubMed 14744536])This 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