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PRODH Monoclonal Antibody (OTI1H6), TrueMAB™, OriGene

Mouse Monoclonal Antibody
Supplier: OriGene TA810559

Description
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.Specifications
PRODH | |
Monoclonal | |
1 mg/mL | |
PBS with 1% BSA, 50% glycerol and 0.02% sodium azide | |
O43272 | |
PRODH | |
Full length human recombit protein of human PRODH produced in E.coli. | |
100 μL | |
Primary | |
Human | |
Antibody | |
IgG1 |
Immunohistochemistry (Paraffin), Western Blot | |
OTI1H6 | |
Unconjugated | |
PRODH | |
HSPOX2, PIG6, POX, PRODH1, PRODH2, TP53I6 | |
Mouse | |
Affinity Chromatography | |
RUO | |
5625 | |
-20° C, Avoid Freeze/Thaw Cycles | |
Liquid |
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