Gamma Tubulin mouse Monoclonal Antibody(7B1), 50ul Fluorescent Staining Mutations in this gene are

Mutations in this gene are associated with autosomal dominant polycystic kidney disease type 2

A related pseudogene has been identified on chromosome 12

Mutations in this gene result in alpha-2-plasmin inhibitor deficiency| which is characterized by severe hemorrhagic diathesis

Constitutive activation of PRKACA caused either by somatic mutations

Stimulates promoter activity in the presence of NFKB2/p49

Gamma Tubulin mouse Monoclonal Antibody(7B1), 50ul Fluorescent Staining Mutations in this gene areThis gene encodes a member of the tubulin superfamily. The encoded protein localizes to the centrosome where it binds to microtubules as part of a complex referred to as the gamma tubulin ring complex. The protein mediates microtubule nucleation and is required for microtubule formation and progression of the cell cycle. A pseudogene of this gene is found on chromosome 7.