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Allfastra Respiratory Bacteria Panel (3) Real Time PCR Kit
Molecular testing procurement depends less on a catalogue name than on sample types, run time, storage, and regulatory status. This Bioperfectus panel states all five.
Respiratory molecular testing sits at the intersection of sample collection, laboratory throughput, and cold-chain handling. The Allfastra Respiratory Bacteria Panel (3) Real Time PCR Kit is presented as a CE-IVD laboratory product from Bioperfectus for detecting three named bacterial targets.
The stated targets are Pseudomonas aeruginosa, Group A Streptococcus, and Staphylococcus aureus. The listed limit of detection is 5 copies/reaction, with an assay runtime of 46 minutes.
Accepted sample types are nasopharyngeal swab, sputum, and bronchoalveolar lavage fluid. Storage is specified at -20±5°C, and shelf life is 12 months.
Two kit formats are listed: YJB20305NW-25T at 25 tests per kit and YJB20305NW-50T at 50 tests per kit. That choice affects order volume, freezer space, and how frequently reagents are opened.
The product page identifies CE-IVD status. Buyers still need to confirm that this marking matches their own jurisdiction, reporting requirements, and laboratory validation procedures.
The kit is supplied for trained personnel following instructions for use, laboratory procedures, and local regulatory requirements. Sourcing, configuration, MOQ, and logistics support are available through Scientific China.
In practice, the 46-minute runtime and 5 copies/reaction limit may matter more for daily scheduling than the headline target list. Procurement should focus on documentation and fit.
Why it matters:
For laboratory buyers, the key checks are target coverage, sample-type compatibility, cold-chain capacity, and CE-IVD recognition in the destination market. Those determine whether the kit can move from quotation to routine use.
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