S6A19 Polyclonal Antibody, 20ul Cryopreservation a repair-deficient mutant that exhibits

a repair-deficient mutant that exhibits hypersensitivity to a number of different DNA-damaging agents

Mutations in this gene have been associated with a predisposition to atypical hemolytic uremic syndrome

Mutations in this gene have been shown to cause an X-linked dominant STAR syndrome that typically manifests syndactyly

and a low-affinity receptor for IgE

S6A19 Polyclonal Antibody, 20ul Cryopreservation a repair-deficient mutant that exhibitsThis gene encodes a system B(0) transmembrane protein that actively transports most neutral amino acids across the apical membrane of epithelial cells. Mutations in this gene result in Hartnup disorder.