该OPLAH Polyclonal Antibody. The protein encoded by this gene acts as a homodimer, using ATP hydrolysis to catalyze the conversion of 5-oxo-L-proline to L-glutamate. Defects in this gene are a cause of 5-oxoprolinase deficiency (OPLAHD).
应用类型
WB
免疫原
Recombinant fusion protein of human OPLAH (NP_060040.1).
