RT-LAMP test kit for viral hemorrhagic septicemia virus
A technology of RT-LAMP and viral hemorrhage, applied in the field of molecular biology, can solve the problems of long detection period, unsuitable for rapid detection, etc., and achieve the effects of simple operation, mild conditions and high sensitivity
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Embodiment 1
[0041] Establishment of RT-LAMP detection kit for viral hemorrhagic sepsis virus
[0042] RT-LAMP detection kit for viral hemorrhagic sepsis virus, including RT-LAMP primer set, RT-LAMP reaction solution, Bst DNA polymerase, AMV reverse transcriptase, positive control and negative control.
[0043](1), RT-LAMP primer design: with the envelope glycoprotein gene (gly G gene, GenBank accession number DQ401190.1) of viral hemorrhagic sepsis virus (VHSV) as the target gene, use the online design software Primer Explorer version4( http: / / primerexplorer.jp / e) to design LAMP primers. The primer sequences are listed in Table 1.
[0044] Table 1 Primer sequence list
[0045]
[0046] (2) RT-LAMP reaction solution: containing 10mM dNTP, 10×ThermoPol reaction buffer, and 150mM MgSO4 aqueous solution, the volume ratio of the three is 8:5:2.
[0047] (3), positive control is the T vector clone that contains viral hemorrhagic septicemia virus (VHSV) envelope glycoprotein gene fragment,...
Embodiment 2
[0054] ESE-Quant tube scanner detection
[0055] Except that the chromogen (SYBR Green I) not in Example 1 is added in the kit, all the others are the same as Example 1.
[0056] Detect viral hemorrhagic septicemia virus (VHSV) by the following method with above-mentioned kit:
[0057] (1) Extraction of the RNA of the sample to be tested: the RNA of the sample to be tested is extracted and purified using a viral RNA extraction kit;
[0058] (2) Constant temperature gene amplification reaction: 25μl reaction system contains: VHSV-F3 0.2μM, VHSV-B30.2μM, VHSV-FIP 1.6μM, VHSV-BIP 1.6μM, VHSV-LF 0.8μM, VHSV-LB 0.8μM , 12.5 μl of RT-LAMP reaction solution, 1U of AMV reverse transcriptase, 8U of Bst DNA polymerase, 0.5 μl of 10×SYBR Green I, 1 to 100 ng of RNA to be tested, filled up to 25 μl with DEPC water; set positive and negative controls; Mix the prepared PCR tube and centrifuge, react at 65°C for 60 minutes, and continue at 80°C for 2 minutes;
[0059] (3) Judgment of resu...
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