Influenza A Virus/Influenza B Virus Nucleic Acid Detection Kit (Fluorescence RT-PCR)
BI-BSJ-04
Herpes simplex virus belongs to the α subfamily of human Herpesviridae. Based on the variation in its G proteins, the virus can be divided into two serotypes: Herpes Simplex Virus Type 1 (HSV1, oral herpes) and Herpes Simplex Virus Type 2 (HSV2, genital herpes). Nucleic acid sequences of the two types are highly homologous, but their infection routes and clinical manifestations are different.
The recurrence rate of HSV2 infection is also much higher than that of HSV1 infection. It is of tremendous clinical importance to be able to diagnose and specifically detect HSV. The primer in this kit is designed to probe the conserved sequences of HSV1 and HSV2 with high specificity to ensure the accuracy of the detection. A human internal reference is included in the kit to ensure the integrity of the entire test process, from specimen collection to transportation, nucleic acid extraction and PCR amplification. UDG enzyme anti-contamination is also added to the kit to prevent false positive results caused by product contamination.
Product Features
- Strong applicability: suitable for pharyngeal swabs.
- High sensitivity: reagent detection sensitivity up to 200 copies/mL.
- Strong specificity: no cross-reaction with a variety of common respiratory tract infection pathogens such as meningococci, Haemophilus influenzae, etc. Endogenous inhibitors (blood, mucin, nasal secretions, etc.) and exogenous inhibitors (dexamethasone, budesonide, etc.) in the samples had no significant effect on the test results.
- High accuracy: The kit can simultaneously detect influenza A virus subtypes: A H1N1, A H1N1 (2009), A H3N2, A H5N1, A H7N9; influenza B virus: Victoria strain and Yamagata strain. The positive and negative coincidence rates were 100% and 100% respectively.
- Simple operation: one-step method to complete RT-qPCR, fully closed tube amplification and detection to prevent aerosol pollution. The detection can be completed within 35 min.
