XRCC2 Polyclonal Antibody, 100ul Petri Dishes Mutations in this gene cause

Mutations in this gene cause Gitelman syndrome| a disease similar to Bartter's syndrome| that is characterized by hypokalemic alkalosis combined with hypomagnesemia| low urinary calcium| and increased renin activity associated with normal blood pressure

™ Mouse IL-4 One-Step ELISA Kit

Polymorphisms in this gene have been linked to various human diseases| including IgA deficiency| common variable immunodeficiency| and premature ovarian failure

The protein encoded by this gene localizes to centrosomes

It has been shown to mediate the immunosuppressive signal of interleukin 10

XRCC2 Polyclonal Antibody, 100ul Petri Dishes Mutations in this gene causeXRCC2 encodes a member of the RecA Rad51 related protein family that participates in homologous recombination to maintain chromosome stability and repair DNA damage. This gene is involved in the repair of DNA double strand breaks by homologous recombination and it functionally complements Chinese hamster irs1, a repair deficient mutant that exhibits hypersensitivity to a number of different DNA damaging agents.