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Leishmania Real Time PCR Kit
Leishmania molecular testing depends on sample type, workflow fit, and local regulatory acceptance. The Bioperfectus kit is listed as CE-IVD in two pack sizes.
The kit is intended for molecular diagnostic testing related to Leishmania by trained personnel. Its stated sample types are whole blood and bone marrow biopsy, using a 5 µL template input.
Published specifications include a limit of detection of 5 copies/reaction and a 62-minute testing time. Labs should confirm these figures against their extraction platform and thermocycler.
Storage is -20±5°C with a 12-month shelf life, so cold-chain planning and inventory turnover matter. Catalog options are 25T/Kit and 50T/Kit.
CE-IVD status does not by itself establish suitability for every market or clinical setting. Buyers should verify local registration, intended use, language requirements, and the current instructions for use.
Procurement should also confirm controls, instrument compatibility, sample-validation requirements, minimum order quantity, and delivery terms. The supplied page does not detail these points.
For operational buyers, the main question is whether the assay can be validated and sustained within the existing laboratory workflow, not simply whether the catalog item is available.
Why it matters:
Pack size affects waste and reorder cycles. Local status, storage, and workflow fit should be resolved before purchase.
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