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catalyzes cleavage of 5-oxo-L-proline to form L-glutamate and is coupled to the hydrolysis of ATP to ADP and inorganic phosphate. Additionally we are shipping 5-Oxoprolinase (ATP-Hydrolysing) Antibodies (11) and 5-Oxoprolinase (ATP-Hydrolysing) Proteins (3) and many more products for this protein.
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In this study, clinical, biochemical, and genetic aspects of five Chinese 5-oxoprolinuria patients with OPLAH or GSS (show GSS ELISA Kits) gene mutations were investigated.
the cause of cellular ATP depletion in nephrotic cystinosis may be the futile cycle (show LRMP ELISA Kits), formed between two ATP-dependant gamma-glutamyl cycle enzymes, gamma-glutamyl cysteine synthetase and 5-oxoprolinase
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).
, 5-oxoprolinase (ATP-hydrolysing)