|Western Blot (WB)||1:500-1:3000|
|Tested Species reactivity||Human|
|Host / Isotype||Rabbit / IgG|
|Immunogen||Recombinant fragment corresponding to a region within amino acids 50 and 235 of Human PRODH|
|Purification||Antigen affinity chromatography|
|Storage buffer||PBS, pH 7, with 1% BSA, 20% glycerol|
|Storage conditions||-20° C, Avoid Freeze/Thaw Cycles|
PA5-27706 targets PRODH in WB applications and shows reactivity with Human samples.
The PA5-27706 immunogen is recombinant fragment corresponding to a region within amino acids 50 and 235 of Human PRODH.
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.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: HSPOX2; mitochondrial; p53-induced gene 6 protein; PIG6; POX; PRODH1; PRODH2; proline dehydrogenase; proline dehydrogenase (oxidase) 1; proline dehydrogenase 1; Proline dehydrogenase 1, mitochondrial; Proline oxidase; Proline oxidase 2; proline oxidase, mitochondrial; SCZD4; TP53I6; tumor protein p53 inducible protein 6
Gene Aliases: HSPOX2; PIG6; POX; POX2; PRODH; PRODH1; PRODH2; TP53I6
UniProt ID: (Human) O43272
Entrez Gene ID: (Human) 5625
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