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Avian Influenza Virus H7 Universal/ HPAI-H7/N9 Subtype RNA Detection Kit
Avian influenza surveillance depends on timely RNA detection in poultry and wild-bird populations. The kit’s stated H7 and HPAI-H7/N9 targets, CE marking, and PCR-platform compatibility define the first procurement questions: sample fit, extraction workflow, and instrument access.
Outbreak response relies on respiratory specimen testing. This kit is listed as a fluorescence PCR method for avian influenza virus RNA, with catalog numbers for 25-test and 50-test formats.
The stated specimen types include throat swabs, nasal swabs, nasopharyngeal extracts, pharyngeal aspirate, and nasal lotion. Laboratories should confirm these match their collection protocols and local validation requirements.
The kit covers H7 Universal and HPAI-H7/N9 subtype targets. H7 viruses have been reported to infect humans, and H5 and H7 highly pathogenic avian influenza can cause poultry losses, so surveillance has both animal-health and public-health relevance.
Technical specifications list sensitivity of 500 copies/mL, storage from -25°C to -15°C for 12 months, and compatibility with ABI7500 and Tianlong Gentier 96E real-time PCR systems. These constraints shape instrument capacity and cold-chain planning.
An internal control is cited to reduce false-negative risk, and the supplier notes use with a Tianlong nucleic acid extraction kit. Buyers should verify extraction compatibility and documented performance rather than assume workflow integration.
CE marking is listed. Procurement teams should still request certificates, lot release information, expiration dating, and any country-specific import or diagnostic-use documentation before committing.
Why it matters:
For avian influenza programs, kit selection is an operational decision. Confirming specimen validation, extraction fit, PCR platform access, and documentation before purchase reduces the risk of stock that cannot be deployed during an outbreak.
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