PRMT1 Monoclonal Antibody, 100ul Hepatocytes It is also known to

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

tissue specificity:Widely expressed with highest levels in the heart

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

regulate the concentrations of individual nucleotides and of nucleotide ratios in response to changing circumstances (Abdelraheim et al

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

PRMT1 Monoclonal Antibody, 100ul Hepatocytes It is also known toThis 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