LAMP (Loop-Mediated Isothermal Amplification) detection primer pair for Seneca valley virus and detection method of Seneca valley virus
A detection method and detection primer technology, applied in the direction of microorganism-based methods, biochemical equipment and methods, microorganism measurement/testing, etc., can solve the problem of no rapid diagnostic method
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[0031] 1 Materials and methods
[0032] 1.1 Viruses, recombinant plasmids and disease materials
[0033] Viruses: SVV L16 strain, PRRSV, PCV2, porcine pseudorabies virus (PRV), swine fever virus (CSFV), porcine epidemic diarrhea virus (PEDV) were all isolated by the Key Laboratory of Animal Bacteriology, Ministry of Agriculture, Nanjing Agricultural University, Store at -20°C.
[0034] Recombinant plasmid: pTOPO-SVV-A (containing SVV P1 gene fragment), the concentration is 500 ng·μL -1 , gene copy number is 1x10 9 copies μL -1 , constructed and provided by the Key Laboratory of Animal Bacteriology, Ministry of Agriculture, Nanjing Agricultural University, stored at -20°C.
[0035] Clinical samples: 10 samples of vesicles from the trotters with SVV clinical onset, collected by the Key Laboratory of Animal Bacteriology, Ministry of Agriculture, Nanjing Agricultural University, and stored at -20°C.
[0036] Viral Nucleic Acid Extraction
[0037] SVV, PRRSV, PEDV, and CSFV ...
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