C9 Polyclonal Antibody, 50ul Mechanical Pipette Defects in this gene are

Defects in this gene are a cause of 3M syndrome type 1 (3M1)

It has also been suggested to be a regulator of cell growth

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

and development

This protein is a small core-associated protein and a subunit of ubiquinol-cytochrome c reductase complex III| which is part of the mitochondrial respiratory chain

C9 Polyclonal Antibody, 50ul Mechanical Pipette Defects in this gene areC9 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.