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- Tel: 858.663.9055
- Email: info@nsjbio.com
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).
Optimal dilution of the OPLAH antibody should be determined by the researcher.
E. coli-derived recombinant human protein (amino acids H788-E1072) was used as the immunogen for the OPLAH antibody.
After reconstitution, the OPLAH antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
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