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Allfastra Respiratory Bacteria Panel (7) Real Time PCR Kit
Respiratory panels compete on turnaround time, sample flexibility, and cold-chain discipline. The documented figures here — 46 minutes, three specimen types, and a seven-target list — set the terms a laboratory must check before ordering.
The Allfastra Respiratory Bacteria Panel (7) Real Time PCR Kit is listed as a Bioperfectus molecular diagnostic product carrying CE-IVD status. Its stated targets are Haemophilus influenzae, Mycoplasma pneumoniae, Legionella pneumophila, Klebsiella pneumoniae, Streptococcus pneumoniae, Bordetella parapertussis and Bordetella pertussis.
Accepted sample types are nasopharyngeal swab, sputum and bronchoalveolar lavage fluid. The limit of detection is given as 5 copies per reaction, with an assay runtime of 46 minutes — a figure that matters when a laboratory schedules runs against shift patterns rather than batch size alone.
Two catalogue configurations exist: YJB110701NW-25T at 25 tests per kit and YJB110701NW-50T at 50 tests per kit. Storage is specified at -20±5°C with a 12-month shelf life, so freezer capacity and consumption rate drive the choice between the two pack sizes.
Procurement teams should confirm minimum order quantity, shipping conditions and whether the extraction platform in use is validated for these specimen types. The product page ties use to trained personnel, applicable instructions for use, laboratory procedures and local regulatory requirements.
That framing matters because CE-IVD marking does not automatically transfer across jurisdictions; a buyer still has to verify local registration status, import documentation and lot-specific certificates before the kit enters routine testing.
Why it matters:
A 12-month shelf life at -20°C makes order sizing a genuine planning decision, not a formality. Verify pack size, cold-chain terms and local registration before committing to volume.
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