AIM2 Polyclonal Antibody, 100ul Protein Post-translational Modification Mutations in this gene have

Mutations in this gene have been identified as the cause of congenital merosin-deficient muscular dystrophy

Highly similar proteins in other organisms are involved in the transduction of signals from Ras to Rac and growth factor-mediated actin remodeling

The laminar organization of multiple neuronal types in the cerebral cortex is required for normal cognitive function

while alpha-globin is produced throughout fetal and adult life

AIM2 Polyclonal Antibody, 100ul Protein Post-translational Modification Mutations in this gene haveAIM2 is a member of the IFI20X IFI16 family. It plays a putative role in tumorigenic reversion and may control cell proliferation. Interferon gamma induces expression of AIM2.