CMC2 Polyclonal Antibody, 100ul Custom Peptide Synthesis Mutations in this gene are

Mutations in this gene are associated with autosomal recessive retinitis pigmentosa

also known as inherited thrombophilia

It is a tetramer made up of alpha-beta dimers linked in a head-to-head arrangement

Prelamin A is farnesylated and carboxymethylated on the cysteine residue of a carboxyl-terminal CaaX motif

CMC2 Polyclonal Antibody, 100ul Custom Peptide Synthesis Mutations in this gene areThis gene is a member of the mitochondrial carrier family. The encoded protein contains four EF hand Ca(2+) binding motifs in the N terminal domain, and localizes to mitochondria. The protein catalyzes the exchange of aspartate for glutamate and a proton across the inner mitochondrial membrane, and is stimulated by calcium on the external side of the inner mitochondrial membrane. Mutations in this gene result in citrullinemia, type II. Multiple