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PRODH Products

The protein encoded by the PRODH 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)
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9 results for "PRODH" in Products

9 results for "PRODH" in Products

PRODH Products

The protein encoded by the PRODH 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)
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Applications: WB, ELISA
Reactivity: Human
Applications: WB
Reactivity: Human
Applications: IHC, WB, ELISA
Reactivity: Human
Applications: IHC, ELISA
Reactivity: Human
Applications: WB, ELISA, MA, AP, PAGE
Applications: IHC
Reactivity: Human
Applications: WB, ELISA
Reactivity: Human, Mouse, Rat
Applications: WB
Applications: AC
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