S6A19 Polyclonal Antibody, 20ul Cryopreservation The bold red color code

The bold red color code makes identification a breeze

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

DMD patients carry mutations which cause premature translation termination (nonsense or frame shift mutations)

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

Different polymorphic forms

S6A19 Polyclonal Antibody, 20ul Cryopreservation The bold red color codeThis 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.