MRP-L13 Polyclonal Antibody, 100ul Digital Burette Mutations in this gene cause

Mutations in this gene cause myopathy and distal arthrogryposis type 2B

together with SNAP25 (synaptosome-associated protein of 25 kDa)

active enzyme is produced following lipopolysaccharide expression in mature dendritic cells

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

It contains three K-homologous (KH) domains which may be involved in RNA binding

MRP-L13 Polyclonal Antibody, 100ul Digital Burette Mutations in this gene causeMammalian mitochondrial ribosomal protein L 13 (39S ribosomal protein L13 mitochondrial) is encoded by nuclear gene MRPL13 and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and