Anti-OPLAH Polyclonal Antibody, 100.0ul

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).

• Size: 100.0ul
• Molecular Weight: 137kDa
• Physical State: Liquid
• Storage: Store at -20℃. Avoid freeze/thaw cycles.
• Application: WB
• Brand: Saint Michael
• Catalogue No.: K002403P-100.0ul

For laboratory research use only. Not for human or animal consumption, diagnostic or therapeutic use.