PRODH antibody [N1N3]

GeneTex

PRODH antibody [N1N3]

9

Research Use Only

1 mg/ml

IgG

The protein encoded by this gene is a mitochondrial proline dehydrogenase that catalyzes the first step in proline degradation. Defects in this gene are a cause of hyperprolinemia type 1 and possibly susceptibility to schizophrenia 4 (SCZD4). The gene is located on chromosome 22q11.21, a region which has also been associated with the contiguous gene deletion syndromes DiGeorge syndrome and CATCH22 syndrome. [provided by RefSeq]

2°C to 8°C,-20°C

12352203