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

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

Radial spokes| which are regularly spaced along cilia| sperm| and flagella axonemes| consist of a thin 'stalk' and a bulbous 'head' that form a signal transduction scaffold between the central pair of microtubules and dynein

and development

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

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.