RPB3 Polyclonal Antibody, 20ul Nucleic Acid Extraction Mutations in this gene cause

Mutations in this gene cause two forms of inherited human muscle disorders: recessive generalized myotonia congenita (Becker) and dominant myotonia (Thomsen)

This gene encodes a secreted chemotactic protein that initiates chemotaxis via the ChemR23 G protein-coupled seven-transmembrane domain ligand

Contains 13 laminin EGF-like domains

This protein can regulate the expression of many xenobiotic metabolizing enzymes

MIM 179508) have regulatory roles in the formation

RPB3 Polyclonal Antibody, 20ul Nucleic Acid Extraction Mutations in this gene causeThis gene encodes the third largest subunit of RNA polymerase II, the polymerase responsible for synthesizing messenger RNA in eukaryotes. The product of this gene contains a cysteine rich region and exists as a heterodimer with another polymerase subunit, POLR2J. These two subunits form a core subassembly unit of the polymerase. A pseudogene has been identified on chromosome 21.