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Hendra Virus Real Time PCR Kit
Hendra virus testing sits in a narrow public-health and reference-lab workflow. For the Bioperfectus kit, the supplied information centers on RUO status, package size, and a defined PCR run profile rather than clinical validation claims.
Labs sourcing rare-pathogen PCR reagents often balance assay availability against documentation and regulatory scope. The Hendra Virus Real Time PCR Kit is listed as a Bioperfectus molecular diagnostic product with RUO status.
The stated use is molecular diagnostic testing related to Hendra Virus. It is supplied for trained personnel following the applicable instructions for use, laboratory procedures, and local regulatory requirements.
The listing reports a LOD of 5 copies/reaction, 5 μL sample input, and sample types including human serum, cerebrospinal fluid, and throat swabs. It also states a 79-minute testing time, -20±5℃ storage, and a 12-month shelf life. These are product-page specifications and should be checked against the current IFU.
Two catalog configurations are shown: YJC70120NW-25T at 25T/Kit and YJC70120NW-50T at 50T/Kit. Buyers should confirm package size, minimum order quantity, availability, delivery options, and a formal quotation through Scientific China.
The supplied input does not state extraction platform, PCR instrument compatibility, internal controls, or regulatory clearance. Those gaps matter for validation, documentation, and procurement review.
For RUO assays, the practical question is not only sensitivity. Documentation, cold-chain handling, and workflow fit determine whether the kit can support the intended laboratory use.
Why it matters:
Buyers should verify RUO limitations, IFU performance, and instrument or extraction compatibility before committing, because those factors decide whether the kit can enter an existing diagnostic workflow.
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