PRMT1 Monoclonal Antibody, 100ul Hepatocytes and provides the primary link

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

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

where ligand-receptor interactions can result in the activation of

PRMT1 Monoclonal Antibody, 100ul Hepatocytes and provides the primary linkThis 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