Pan Methyl Lysine Polyclonal Antibody, 20ul Hepatocytes Defects in PEX19 are a

Defects in PEX19 are a cause of Zellweger syndrome (ZWS)

It contains N-terminal sites for myristylation and palmitylation

Defects in this gene cause autosomal dominant spinocerebellar ataxia 12 (SCA12)

Play an inhibitory role on IL13 signaling by binding to IL13RA1

Induces cell cycle arrest and mediates apoptosis by caspase activation and in p53-independent manner

Pan Methyl Lysine Polyclonal Antibody, 20ul Hepatocytes Defects in PEX19 are aLysine methylation occurs in three distinct states, having either one (me1), two (me2) or three (me3) methyl groups attached to the amine group of the lysine side chain. In eukaryotes, histone H3 trimethylated at lysine 4 (H3K4me3) is associated with active chromatin and gene expression.