Caspase 3 p17 Polyclonal Antibody, 100ul Supplements and defective GRIA2 RNA editing

and defective GRIA2 RNA editing at the Q/R site may be relevant to amyotrophic lateral sclerosis (ALS) etiology

differing only in the translation start site used

GO annotations related to this gene include actin binding and calmodulin binding

By acetylating histones

and tropomyosin

Caspase 3 p17 Polyclonal Antibody, 100ul Supplements and defective GRIA2 RNA editingThis gene encodes a protein which is a member of the cysteine aspartic acid protease (caspase) family. Sequential activation of caspases plays a central role in the execution phase of cell apoptosis. Caspases exist as inactive proenzymes which undergo proteolytic processing at conserved aspartic residues to produce two subunits, large and small, that dimerize to form the active enzyme. This protein cleaves and activates caspases 6, 7 and 9, and the