mouse liver tissue were subjected to SDS PAGE followed by western blot with FNab06796(PRODH antibody) at dilution of 1:1000
Immunohistochemistry of paraffin-embedded human liver injury using FNab06796( PRODH Antibody) at dilution of 1:50
Background
This gene encodes a mitochondrial protein that catalyzes the first step in proline degradation. Mutations in this gene are associated with hyperprolinemia type 1 and susceptibility to schizophrenia 4 (SCZD4). This gene is located on chromosome 22q11.21, a region which has also been associated with the contiguous gene deletion syndromes, DiGeorge and CATCH22. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.