Nucleic acid detection kit for influenza A virus and influenza B virus and use method of nucleic acid detection kit

A technology of influenza B virus and influenza A virus, which is applied in the direction of biochemical equipment and methods, and the measurement/inspection of microorganisms, can solve the problems of inconvenient and difficult detection, and the accuracy of results, so as to reduce the background signal value , Improve specificity, fast and simple reaction procedure

Active Publication Date: 2021-12-14
SHANGHAI BIOGERM MEDICAL TECH CO LTD
View PDF4 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] The invention provides a type A and type B influenza virus nucleic acid detection kit and a method of use, which solve the problems that the existing type A and type influenza virus detection is not convenient enough and difficult to evaluate the accuracy of the results

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Nucleic acid detection kit for influenza A virus and influenza B virus and use method of nucleic acid detection kit
  • Nucleic acid detection kit for influenza A virus and influenza B virus and use method of nucleic acid detection kit
  • Nucleic acid detection kit for influenza A virus and influenza B virus and use method of nucleic acid detection kit

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 2

[0109] 1 case of influenza A virus positive sample and 1 case of influenza B positive sample were tested with this kit, the results are as follows figure 1 As shown, both samples are positive for the corresponding channels, indicating that the present invention can effectively detect influenza A and B influenza virus samples, and can correctly type.

Embodiment 3

[0111] Add different concentrations of UNG enzymes to the system: concentration 1 (4.0U / / μL), concentration 2 (6.0U / / μL), optimal concentration (5.0U / μL), at 1×10 4 The products containing dU in copies / mL were amplified as templates. The results showed that the optimal concentration of UNG enzyme had no amplification curve, indicating that 5U / μL of UNG enzyme could eliminate no more than 1×10 4 Copies / mL of the product pollution, play the role of anti-pollution, the test results are as follows Figure 2-3 shown.

Embodiment 4

[0113] Set up 4 different combinations of DNA polymerases, adding Taq enzyme + Tth enzyme (combination 1), Taq enzyme + Vent enzyme + Tth enzyme (combination 2), Taq enzyme + Vent enzyme (combination 3), and only Containing 4 combinations of Taq enzyme (combination 4), comparative detection of influenza A / B positive samples, comparative detection results are as follows Figure 4-5 shown. from Figure 4-5 It can be seen from the results that when Taq enzyme, Vent enzyme and Tth enzyme are added to the system at the same time, the amplification effect of the reaction system is the best.

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

No PUM Login to view more

Abstract

The invention relates to a nucleic acid detection kit for an influenza A virus and an influenza B virus and a use method of the nucleic acid detection kit. The nucleic acid detection kit comprises an influenza A / B virus reaction solution, a positive control solution and a negative control solution, wherein the influenza A / B virus reaction solution contains a plurality of probes with different fluorescence labels, primers, an enzyme mixture, an enhancer, a freeze-drying protective additive, a 10xbuffer, a nucleotide mixture and the like, and can be used for detecting whether the A / B influenza virus is infected or not in the same reaction system. The whole process of sample collection, nucleic acid extraction, amplification and detection is monitored through the endogenous internal reference, and misjudgment caused by false negative results is avoided. When the probe is complete, a quenching group is close to a reporter group in spatial position, so that fluorescence emitted by the reporter group is inhibited. When the primer extends, the probe combined with a template is cut off by Taq enzyme (5 '-> 3' exonuclease activity), the reporter group is separated from the quenching group, and a fluorescence signal is generated, so that the influenza A virus and the influenza B virus are detected on the nucleic acid level.

Description

technical field [0001] The invention relates to the technical field of detection of type A and type B influenza viruses, in particular to a type A and type B influenza virus nucleic acid detection kit and a use method. Background technique [0002] Influenza is an acute respiratory infectious disease caused by influenza virus. It occurs frequently in spring and winter, spreads rapidly, has a high incidence rate, and has a short epidemic period. It is easy to cause outbreaks or pandemics, and it is difficult to control. Influenza viruses include three types: A, B, and C. Type A is the most likely to cause epidemics, followed by Type B, and Type C rarely causes epidemics. Influenza virus is mainly transmitted through air droplets, often causing fever, fatigue, muscle aches and mild to moderate respiratory symptoms, severe cases can cause pneumonia, myocarditis and heart failure. Because the infection symptoms and epidemic characteristics caused by these viruses are similar, i...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
Patent Type & Authority Applications(China)
IPC IPC(8): C12Q1/70C12Q1/686
CPCC12Q1/701C12Q1/686C12Q2600/166C12Q2521/107C12Q2545/101C12Q2545/113C12Q2563/107C12Q2521/531C12Q2527/127
Inventor 赵百慧杨孙孝李春明向军喜
Owner SHANGHAI BIOGERM MEDICAL TECH CO LTD
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products