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

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

Synthetic RNA is an essential research tool widely used in studying gene structure and function

factor XIIa

Co-transcription of this gene and the neighboring downstream gene (NME2) generates naturally-occurring transcripts (NME1-NME2)

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.