Western blot analysis of Mouse liver tissue Mouse brain tissue Rat brain tissue Rat liver tissue and Human fetal liver tissue lysates using QDPR Polyclonal Antibody at dilution of 1:800
Immunohistochemistry of paraffin-embedded Human liver cancer tissue using QDPR Polyclonal Antibody at dilution of 1:70(×200)
Immunohistochemistry of paraffin-embedded Human ovarian cancer tissue using QDPR Polyclonal Antibody at dilution of 1:70(×200)
This gene encodes the enzyme dihydropteridine reductase, which catalyzes the NADH-mediated reduction of quinonoid dihydrobiopterin. This enzyme is an essential component of the pterin-dependent aromatic amino acid hydroxylating systems. Mutations in this gene resulting in QDPR deficiency include aberrant splicing, amino acid substitutions, insertions, or premature terminations. Dihydropteridine reductase deficiency presents as atypical phenylketonuria due to insufficient production of biopterin, a cofactor for phenylalanine hydroxylase.