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Borrelia Burgdorferi Real Time PCR Kit
Laboratories evaluating a Borrelia Burgdorferi PCR kit must match kit format, sample type, and cold-chain requirements to actual testing demand. The listed CE-IVD status is a starting point, not a substitute for local market verification.
The Borrelia Burgdorferi Real Time PCR Kit is a Bioperfectus product listed for molecular diagnostic testing related to Borrelia Burgdorferi. Its stated sample type is human serum, and the product page identifies CE-IVD regulatory status.
Stated performance and workflow figures include a limit of detection of 5 copies/reaction and a 66-minute assay runtime. Those figures matter for batch planning, turnaround expectations, and comparison with existing molecular workflows.
Storage is specified at -20±5°C with a 12-month shelf life. That places the kit in a frozen supply chain, so buyers need to confirm receiving capacity, freezer space, and inventory rotation before committing to a package size.
The kit is catalogued in 25-test and 50-test packages under YJC60113NW codes. Smaller packages can reduce waste for lower-volume or irregular testing, while larger packages may suit scheduled batch testing, subject to verification of actual demand.
The input does not identify compatible real-time PCR instruments, extraction methods, or internal controls. Procurement teams should request the instructions for use and confirm those workflow details, plus local regulatory acceptance, before ordering.
Because the product is intended for trained personnel, documentation and training requirements form part of the purchasing decision. CE-IVD marking alone does not confirm suitability for every laboratory or jurisdiction.
Why it matters:
For molecular labs and distributors, the practical decision rests on sample type, throughput, cold-chain handling, and local regulatory acceptance. Confirming these details before purchase reduces the risk of workflow mismatch or unusable inventory.
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