Bioperfectus Neisseria Gonorrhoeae Real Time PCR Kit: RUO Sourcing in Practice

Neisseria Gonorrhoeae Real Time PCR Kit

Molecular detection of Neisseria gonorrhoeae is routine in sexual health laboratories, where swab and urine workflows are standardised. Kits in this segment are judged on sample compatibility, storage constraints and documentation as much as on assay chemistry.

The Bioperfectus kit, catalog JC60107NW, is supplied as 50 tests per kit with a 5 μL sample input. Stated sample types are male urethral swab, female cervical swab and urine.

The product page reports an LOD of 1×10 4 CFU/mL, 100% sensitivity and 99.88% specificity. These are supplier-stated figures, normally re-checked against a laboratory’s own extraction platform before use.

Regulatory status is listed as RUO. That labelling generally excludes clinical diagnostic reporting in many jurisdictions, so intended use should be checked against local rules before ordering.

Storage at -20±5℃ and transport at -20±8℃, with a 12-month shelf life, place the kit in a frozen supply chain. Dry-ice handling and frozen bench storage constrain order size.

Scientific China lists sourcing, configuration, MOQ and logistics support. Buyers should confirm package size, minimum order quantity, documentation and delivery terms in a formal quotation.

Where RUO status and supplier-reported performance figures apply, the validation burden shifts to the receiving laboratory. Procurement planning should account for that work.

Why it matters:
For operators, RUO labelling and frozen logistics are the two constraints most likely to determine whether the kit fits a given laboratory. Confirm both before committing to volume.

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