The protein encoded by this gene acts as a homodimer, using ATP hydrolysis to catalyze the conversion of 5-oxo-L-proline to L-glutamate. Defects in this gene are a cause of 5-oxoprolinase deficiency (OPLAHD). [provided by RefSeq, Jun 2012]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| OPLAH-20-RE | 20 (40 μL) | 200 μL |  |
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| OPLAH-20-OR | 20 (40 μL) | 200 μL |  |
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| OPLAH-20-GO | 20 (40 μL) | 200 μL |  |
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| OPLAH-20-GR | 20 (40 μL) | 200 μL |  |
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| OPLAH-20-AQ | 20 (40 μL) | 200 μL |  |
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The protein encoded by this gene acts as a homodimer, using ATP hydrolysis to catalyze the conversion of 5-oxo-L-proline to L-glutamate. Defects in this gene are a cause of 5-oxoprolinase deficiency (OPLAHD). [provided by RefSeq, Jun 2012]
Gene Symbol : OPLAH
Gene Name : 5-oxoprolinase, ATP-hydrolysing
Chromosome : CHR 8: 144,064,025-144,051,265
Locus : 8q24.3
Alt. Genes : ZNF263
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