SAP30 Polyclonal Antibody, 20ul 3D Culture Mutations in this gene cause

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 blood pressure

The encoded protein may be important in the regulation of inflammatory response

Conquer the unknown with our Zearalenone Elisa Kit-48T

The protein encoded by this gene has high sequence similarity to the protein encoded by ADAMTS16

The translocation produces a fusion protein which is encoded by sequence from both BCR and ABL

SAP30 Polyclonal Antibody, 20ul 3D Culture Mutations in this gene causeHistone acetylation plays a key role in the regulation of eukaryotic gene expression. Histone acetylation and deacetylation are catalyzed by multisubunit complexes. The protein encoded by this gene is a component of the histone deacetylase complex, which includes SIN3, SAP18, HDAC1, HDAC2, RbAp46, RbAp48, and other polypeptides. This complex is active in deacetylating core histone octamers, but inactive in deacetylating nucleosomal histones. A