Raa constant temperature fluorescent detection primer probe set, kit and method for African swine fever virus cd2v gene
A technology of African swine fever virus and fluorescent probe, applied in the field of molecular biology, to achieve simple and fast response
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Embodiment 1
[0034] Embodiment 1: the design of the RAA constant temperature fluorescence detection primer probe group of African swine fever virus CD2V gene
[0035]This study refers to the African swine fever gene CD2V gene sequence published on GenBank, and uses DNAMAN 6.0 software to compare multiple sequences. A large number of experiments have shown that different primers have a certain influence on the effect and sensitivity of isothermal amplification. Therefore, this study preliminarily designed four sets of primer probes for the African swine fever virus CD2V gene: ASFV-CD2V-1, ASFV-CD2V-2, ASFV-CD2V-3 and ASFV-CD2V-4 (primer sequences are listed in Table 1. shown), these sequences can specifically combine with the corresponding sequences of the African swine fever virus CD2V gene, wherein the size of the target fragment amplified by the above four sets of primers is 107bp, 110bp, 172bp and 197bp respectively, and the positive sample amplification curve is as follows: figure 1 s...
Embodiment 2
[0039] Embodiment 2: RAA constant temperature fluorescent detection kit and detection method of African swine fever virus CD2V gene
[0040] This embodiment provides a kind of RAA thermostatic fluorescence detection kit of ASFV-CD2V, including primer mixture, specific fluorescent probe, A Buffer (20% PEG), B Buffer (280mM MgAc), RAA dry powder reagent, African swine fever Viral standards and ddH 2 O.
[0041] The composition of RAA dry powder reagent is as follows: 1mmol / L dNTP, 90ng / μL SSB protein, 120ng / μL recA recombinase protein (SC-recA / BS-recA) or 30ng / μL Rad51, 30ng / μL Bsu DNA polymerase, 100mmol / L Tricine , 20% PEG, 5mmol / L dithiothreitol, 100ng / μL creatine kinase, Exo exonuclease.
[0042] In the primer mixture described in this embodiment, the base sequence of the forward primer is shown in SEQ ID No.1, the base sequence of the reverse primer is shown in SEQ ID No.2, the forward primer and The molar ratio of the reverse primer is 1:1.
[0043] The specific probe ...
Embodiment 3
[0060] Embodiment 3: Apply the kit of the present invention to carry out actual sample detection
[0061] In order to verify that the primers, probes, and reagents of the present invention can be used normally in actual conditions, the actual conditions are simulated, and the primers, probes, and reagents of the present invention are used to detect actual samples.
[0062] The actual samples are swabs from the mouth and nose of sick pigs and blood samples (serum, plasma and whole blood) of sick pigs, totaling 12. The detection result was consistent with the known PCR detection result, and the coincidence rate was 100%.
[0063] It shows that the primer-probe combination kit of the present invention has the functions of rapid, real-time, sensitive, accurate and convenient detection of African swine fever CD2V gene under body temperature conditions (37°C-39°C) in a fluorescent detection instrument with temperature control function. Advantages of detection.
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