Ribosomal Protein S5 Polyclonal Antibody, 100ul RNA Synthesis and mutations in SCN2A have

and mutations in SCN2A have been linked to several seizure disorders

The protein belongs to the L31E family of ribosomal proteins

Evidence indicates that mutations in this gene are responsible for the primary defects in patients with progressive myoclonic epilepsy (EPM1)

CD2BP2 encodes a bi-functional protein (CD2 cytoplasmic tail binding protein 2)

The encoded preproprotein is secreted by natural killer (NK) cells and cytotoxic T lymphocytes (CTLs) and proteolytically processed to generate the active protease

Ribosomal Protein S5 Polyclonal Antibody, 100ul RNA Synthesis and mutations in SCN2A haveRibosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. RPS5 (ribosomal protein S5) encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S7P family of ribosomal proteins. It is located in the cytoplasm. Variable expression of RPS5 in colorectal