PRMT1 Monoclonal Antibody, 100ul Hepatocytes Mutations in this gene are

Mutations in this gene are associated with neurodegeneration with brain iron accumulation (NBIA)

This gene encodes a multidomain protein containing an N-terminal alpha-helical region with a coiled-coil motif

and provides the primary link between glycolysis and the tricarboxylic acid (TCA) cycle

It is also known to be an entry co-receptor for HIV-1

PRMT1 Monoclonal Antibody, 100ul Hepatocytes Mutations in this gene areThis gene encodes a member of the protein arginine N methyltransferase (PRMT) family. Post translational modification of target proteins by PRMTs plays an important regulatory role in many biological processes, whereby PRMTs methylate arginine residues by transferring methyl groups from S adenosyl L methionine to terminal guanidino nitrogen atoms. The encoded protein is a type I PRMT and is responsible for the majority of cellular arginine methylation