S12A3 Rabbit Polyclonal Antibody, 20ul Oligo Pool unlike the other class I

unlike the other class I PI3Ks

2004 [PubMed 14744536])

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

and NF-kappa-B

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

S12A3 Rabbit Polyclonal Antibody, 20ul Oligo Pool unlike the other class IThis 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