Avian Influenza Virus Subtype H5N2 Real Time PCR Kit: A Procurement Checkpoint

Avian Influenza Virus Subtype H5N2 Real Time PCR Kit

Laboratories comparing real-time PCR reagents typically weigh turnaround time, sample input, storage, and kit configuration against expected testing volume. The Avian Influenza Virus Subtype H5N2 Real Time PCR Kit from Bioperfectus is listed for molecular diagnostic testing related to H5N2.

The supplied specifications state a limit of detection of 5 copies/reaction and a sample input volume of 5 μL. Listed sample types are human throat swab and nasopharyngeal secretions, with a testing time of 79 minutes.

Storage is stated at -20±5°C, with a 12-month shelf life. That places the kit within frozen reagent logistics, where dry-ice handling, freezer capacity, and inventory rotation can affect usable stock.

Two catalog configurations appear: JC10215NW-25T at 25T/Kit and JC10215NW-50T at 50T/Kit. Buyers should match package size to test demand so reagents are not discarded before expiry.

Before purchase, verify the CE-IVD status for the intended market, local registration requirements, extraction and PCR instrument compatibility, and whether the listed human sample types match the laboratory’s validation plan.

Availability, minimum order quantity, delivery options, and formal quotation are handled through Scientific China. Cold-chain shipping and import documentation need confirmation because frozen reagents can be delayed at borders.

A diagnostic kit is not a standalone purchase. Its practical value depends on validation, workflow fit, and reliable replenishment under the stated storage and shelf-life conditions.

Why it matters:
For buyers, the critical checks are regulatory eligibility, sample-type validation, cold-chain capacity, and package size. A kit that fits the laboratory’s volume and logistics will be easier to keep in routine use.

View Product →