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

subunit:Component of the PeBoW complex

The enzyme may localize to the endoplasmic reticulum and the Golgi

™ Mouse IL-4 One-Step ELISA Kit

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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.