Supplementary Tables: Effect of mismatch between types of viral nucleic acid and intended targets of extraction kits on PCR-based testing
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<strong>Supplementary Table 1.</strong> The summary of the designed primer sets information for the detection of respective viruses <strong>Supplementary Table 2. </strong>Composition of the reaction mixture (in µL) for conventional PCR assays performed on nucleic acid extracted from <em>bovine herpesvirus type 1</em> (BHV-1), <em>porcine epidemic diarrhea virus</em> (PEDV), <em>porcine circovirus type 2</em> (PCV-2), and <em>porcine rotavirus type A</em> (PoRVA) <strong>Supplementary Table 3.</strong> PCR conditions for conventional PCR assays performed on nucleic acid extracted from <em>bovine herpesvirus type 1</em> (BHV-1), <em>porcine epidemic diarrhea virus</em> (PEDV), <em>porcine circovirus type 2</em> (PCV-2), and <em>porcine rotavirus type A</em> (PoRVA) <strong>Supplementary Table 4.</strong> Composition of the reaction mixture (in µL) for real-time (r) PCR assays performed on nucleic acid extracted from <em>bovine herpesvirus type 1</em> (BHV-1), <em>porcine epidemic diarrhea virus</em> (PEDV), <em>porcine circovirus type 2</em> (PCV-2), and <em>porcine rotavirus type A</em> (PoRVA) <strong>Supplementary Table 5.</strong> PCR conditions for real-time (r) PCR assays performed on nucleic acid extracted from <em>bovine herpesvirus type 1</em> (BHV-1), <em>porcine epidemic diarrhea virus</em> (PEDV), <em>porcine circovirus type 2</em> (PCV-2), and <em>porcine rotavirus type A</em> (PoRVA) <strong>Supplementary Table 6.</strong> Summary of the amplification sensitivity results of real-time (r) PCR assays



