PRMT1 Monoclonal Antibody, 100ul Hepatocytes another member of the neuregulin

another member of the neuregulin family of ligands

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

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

tissue specificity:Widely expressed with highest levels in the heart

PRMT1 Monoclonal Antibody, 100ul Hepatocytes another member of the neuregulinThis 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