Rabbit Polyclonal antibody to PRODH (proline dehydrogenase (oxidase) 1)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]
Immunogen
Recombinant protein encompassing a sequence within the center region of human PRODH. The exact sequence is proprietary.
Key Feature
Clonality
Polyclonal
Isotype
IgG
Host Species
Rabbit
Tested Applications
WB
*Optimal dilutions/concentrations should be determined by the researcher.
:
Species Reactivity
Human
Predicted Reactivity
Mouse, BovineMouse (84%), Bovine (80%)
Concentration
1mg/ml (Please refer to the vial label for the specific concentration)