Bioperfectus HPV Real Time PCR Kit: What Labs Can Verify Before Ordering

Human Papillomavirus Real Time PCR Kit

HPV molecular testing depends on matching an assay to the sample types a lab already handles and the extraction platform it already runs.

The Bioperfectus kit is a CE-IVD real-time PCR product for HPV-related molecular diagnostic testing, run by trained personnel under local requirements. It uses a 5 μL sample input, lists cervical exfoliated cells, ThinPrep and BD SurePath cytology samples, and cervical swabs, and states a 100-minute testing time.

Reported detection limits differ by genotype: 500 copies/mL for HPV16 and HPV18, and 3000 copies/mL for the other listed types. Stated PPA is 95.19% and NPA 96.59%.

Storage at -20±5°C with a 12-month shelf-life introduces cold-chain constraints that affect order quantity and storage planning.

Two catalog numbers separate extraction compatibility. JC80402-NW-50T pairs with the Bioperfectus DNA extraction kit SDK80120 and SSNP or SMPE-960 automated extractors; JC80402-NWO-50T is listed for other nucleic acid extraction products. The lab’s existing extraction platform, not the PCR instrument alone, determines which applies.

Buyers should verify CE-IVD documentation, local registration, and validated sample-type claims before purchase.

The practical question is whether the kit fits the extraction and sample-handling chain already installed.

Why it matters:
Extraction compatibility and storage conditions determine which catalog number a lab can use.

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