NCPR Polyclonal Antibody, 50ul Hepatocytes and to the T-cell activation

and to the T-cell activation antigen CD26

a proline-rich region

Studies suggest certain mutations in this gene lead to childhood absence epilepsy (CAE)

called muscle acylphosphatase and erythrocyte acylphosphatase on the basis of their tissue localization

NCPR Polyclonal Antibody, 50ul Hepatocytes and to the T-cell activationThis gene encodes an endoplasmic reticulum membrane oxidoreductase with an FAD binding domain and a flavodoxin like domain. The protein binds two cofactors, FAD and FMN, which allow it to donate electrons directly from NADPH to all microsomal P450 enzymes. Mutations in this gene have been associated with various diseases, including apparent combined P450C17 and P450C21 deficiency, amenorrhea and disordered steroidogenesis, congenital adrenal