Bioperfectus Human Papillomavirus Genotyping Real Time PCR Kit in Lab Procurement

Human Papillomavirus Genotyping Real Time PCR Kit

HPV genotyping depends on molecular workflow fit, extraction compatibility, and local regulatory acceptance. The Bioperfectus kit is listed as CE-IVD with defined performance and sample specifications, giving buyers a concrete starting point for verification.

The Bioperfectus Human Papillomavirus Genotyping Real Time PCR Kit is intended for molecular diagnostic testing related to HPV genotyping. It is supplied for trained personnel under the applicable instructions for use, laboratory procedures, and local regulatory requirements.

Published specifications include a limit of detection of 400 copies/mL, PPA of 91.20%, and NPA of 98.20%. Sample input is listed as 2 μL*8, with cervical exfoliated cells in ThinPrep and BD SurePath cytologic samples, plus cervical swabs. Reported testing time is 90 minutes for qualitative and genotyping use; storage is −20±5°C with a 12-month shelf life.

Catalog variants separate extraction compatibility. JC80301NW formats are compatible with Bioperfectus DNA extraction kit SDK80120 and automatic extractors SSNP series and SMPE-960. JC80301NWO formats are compatible with other nucleic acid extraction products. Buyers should match catalog number to their extraction platform before ordering.

Because the kit is supplied under local requirements, documentation and logistics need early checks. Procurement should verify CE-IVD scope in the destination market, IFU language, package size, minimum order quantity, lead time, and cold-chain handling for −20°C storage.

The practical question is whether the assay fits the installed extraction base, expected sample mix, and regulatory pathway. A quotation request should include instrument model, sample type, monthly volume, and required regulatory documents.

Why it matters:
For laboratories, extraction compatibility and verified local acceptance should be confirmed before price comparison.

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