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Mycobacterium Tuberculosis Real Time PCR Kit
Molecular TB testing depends on cold-chain, trained staff, and regulatory fit as much as assay performance. The kit’s CE-IVD status and sputum sample format shape how labs evaluate it.
The Mycobacterium Tuberculosis Real Time PCR Kit is a Bioperfectus molecular diagnostic product listed for CE-IVD use. Its stated workflow covers sputum samples, with an assay runtime of 75 minutes and a limit of detection of 5×10 2 copies/mL.
The kit is supplied for trained personnel following instructions for use, laboratory procedures, and local regulatory requirements. Storage is specified at -20±5℃ with a 12-month shelf life, making freezer capacity and inventory rotation part of normal planning.
Two catalog configurations are listed: JB20123NW-25T at 25 tests per kit and JB20123NW-50T at 50 tests per kit. That choice affects run scheduling, waste, and the frequency of reagent lot changes.
Procurement teams should verify CE-IVD recognition in their jurisdiction, because the product page identifies regulatory status but does not replace local market clearance. Documentation for instructions, performance claims, and biosafety handling should be reviewed before ordering.
Scientific China lists sourcing, configuration, MOQ, and logistics support. Buyers should confirm whether cold-chain shipping is available and whether the receiving laboratory can maintain the required storage temperature.
For TB testing programs, test volume, sample throughput, and local reporting requirements will determine whether either kit size fits. The analytical value of a real-time PCR kit depends on the full laboratory system around it.
Why it matters:
Buyers should match kit format to actual sputum-testing volume and confirm regulatory acceptance, cold-chain handling, and shelf life before committing to a package size.
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