Siniperca chuatsi infectious spleen and kidney necrosis virus (ISKNV) inactivation rapid detection kit and detection method
A technology for spleen and kidney necrosis virus and its detection method, which is applied in the field of rapid detection kits for the inactivation of infectious spleen and kidney necrosis virus, to achieve the effects of shortening the production cycle and improving production efficiency
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[0027] 1. Screening of target genes
[0028] According to the transcription profile results of ISKNV-infected CPB cells in our laboratory, five viral ORFs with the highest expression levels were selected, and specific primers and probes were designed using Primer 5.0 software (see Table 1). ISKNV was serially diluted to 1, 10, 100, and 1000 copies / mL and inoculated into T25 cell culture flasks respectively. Seven days after inoculation, total RNA was extracted and reverse-transcribed to prepare cDNA templates. Using Premix Ex Taq TM (Probe qPCR) kit was used to detect the expression levels of these genes. Reaction system: Add 10 μL of Mix, 0.4 μL of ROX, 0.4 μL of each 10 μmol / L primer ISKNV FP / ISKNV RP, 0.4 μL of 10 μmol / L probe ISKNV probe, 2 μL template, and replenish water to 20 μL. In the negative control group, the samples to be tested were replaced with deionized water. The reaction conditions were: 95°C for 30s, 1 cycle; 95°C for 5s, 60°C for 34s, 40 cycles, and the...
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