C9 Polyclonal Antibody, 50ul Mechanical Pipette Mutations in PLCG2 have been

Mutations in PLCG2 have been found in autoinflammation

presumably by hydrolysis of the high molecular mass seminal vesicle protein

There are a number of related genes present on chromosomes 20 and 22

and development

This gene encodes a member of a family of proteins that possess a 100-amino acid PDZ domain at the N terminus and one to three LIM domains at the C-terminus

C9 Polyclonal Antibody, 50ul Mechanical Pipette Mutations in PLCG2 have beenC9 encodes the final component of the complement system. It participates in the formation of the Membrane Attack Complex (MAC). The MAC assembles on bacterial membranes to form a pore, permitting disruption of bacterial membrane organization. Mutations in C9 cause component C9 deficiency.