CMC2 Polyclonal Antibody, 100ul Custom Peptide Synthesis Prelamin A is farnesylated and

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

Diseases associated with TMBIM4 include lassa fever and venezuelan hemorrhagic fever

Alternatively spliced transcript variants have been reported

Mutations in this gene are associated with autosomal recessive retinitis pigmentosa

also known as inherited thrombophilia

CMC2 Polyclonal Antibody, 100ul Custom Peptide Synthesis Prelamin A is farnesylated andThis 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