Quick Entrance
CN | Japanese

Respiratory infection is one of the most common diseases, with adolescents and adults being infected about 2-4 times a year, and children being infected about 6-8 times a year. It is usually accompanied by acute inflammation of the nasal cavity, pharynx, or throat, with most infections being viral, except for a few bacterial infections. SARS-CoV-2 Virus, Respiratory Syncytial Virus, Influenza A Virus and Influenza B Virus have strong transmission power. Epidemiological and clinical symptoms are very similar. Double transmission increases the difficulty of epidemic prevention and control. Therefore, it is an important guarantee for people's health to carry out the detection of COVID-19, influenza virus and other pathogens, do a good job in differential diagnosis, and take targeted prevention and control measures in time.

Product Details FAQ Specification Instructions

This kit uses highly conserved regions of SARS-CoV-2 Virus, Respiratory Syncytial Virus, Influenza A Virus and Influenza B Virus, and designs specific primer probes. The primers and probes can specifically bind to the target sequence. Under the action of reverse transcriptase and hot start Taq DNA polymerase, this segment is specifically amplified, and the fluorescent probe is hydrolyzed during amplification to generate fluorescence. The detection system contains dUTP-UDG enzyme to fully degrade potential product contamination and avoid false positive results; In addition, internal standards are set up to monitor the entire process of sample collection, transportation, nucleic acid extraction, and PCR amplification for highly conserved regions on the human genome, avoiding false negative results and ensuring the effectiveness of the entire process.


This kit can qualitatively detect the nucleic acids of SARS-CoV-2, Respiratory Syncytial Virus, Influenza A Virus, Influenza B Virus, providing information for clinical diagnosis; the detection system contains dUTP-UDG enzyme anti-contamination measures, which can avoid false positive results; At the same time, human-derived internal references are introduced to monitor the entire process of specimen collection, transportation, nucleic acid extraction, and PCR amplification to avoid false negative results; it takes only 35 minutes to complete detection and issue report.

Applicability
Suitable for nasopharyngeal swab sample.
High sensitivity
Three different batches of reagents were used to test, and the detection sensitivity was 500 copies/mL.
High accuracy
It can quickly detect SARS-CoV-2, Respiratory Syncytial Virus, Influenza A Virus, Influenza B Virus. Reference material testing results: positive coincidence rate of 100%, negative coincidence rate of 100%.
Easy to operate
PCR amplification and detection done in completely closed tube to prevent aerosol contamination.


The kit is used for the auxiliarydiagnosis and epidemiological surveillance of SARS-COV-2, RSV,Flu A and FluB infection, cannot be used as the basis for the diagnosis or exclusion of cases alone.



1. The kit should be stored at -25°C ~ -15°C away from light and avoid repeated freeze-thaw.

2. The kit can be stored for 3 days at 2-8°C after opening.

3. The kit can be stored for up to 12 months if all components are kept in the manner above. Do not use after the stated expiry date.

4. The kit can be transported in foam box sealed with ice bags or dry ice under 8°C.