AQP10 Polyclonal Antibody, 50ul Electrophoresis & Labeling mutations in this gene can

mutations in this gene can cause autosomal recessive neuromyotonia and axonal neuropathy

The encoded protein may be involved in the activation of lymphoid cells and support testicular functions

Also interacts with CDK4

Nibrin is a member of the MRE11/RAD50 double-strand break repair complex which consists of 5 proteins

Caspase 3 cleaves and activates caspases 6

AQP10 Polyclonal Antibody, 50ul Electrophoresis & Labeling mutations in this gene canThis gene encodes a member of the aquaglyceroporin family of integral membrane proteins. Members of this family function as water permeable channels in the epithelia of organs that absorb and excrete water. This protein was shown to function as a water selective channel, and could also permeate neutral solutes such as glycerol and urea.