Rockfish viral nerve necrosis virogene diagnostic kit and detecting method thereof
A technology for nerve necrosis and genetic diagnosis, which is applied in biochemical equipment and methods, and microbial measurement/inspection, etc., can solve problems such as difficulty in popularization, troublesome material preparation, and low sensitivity, so as to improve scientific management efficiency and avoid virus transmission and epidemics , Guaranteed rapid effect
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Embodiment 1
[0024] Embodiment 1: Gene diagnostic kit of grouper viral neuronecrosis virus 1. RNA extraction liquid (A liquid), 2 tubes, 5ml / tube, Trizol liquid is installed inside. 2. Solution B, self-prepared, mainly chloroform, 200μl / part x 10 parts, 2ml in total. 3. Solution C, self-prepared, mainly isoamyl alcohol, 500μl / part x 10 parts, 5ml in total. 4. Liquid D, self-prepared, mainly 70% ethanol, 1ml / part x 10 parts, 10ml in total. 5. Liquid E, 1 tube, 0.5ml / tube, filled with DEPC water. 6. RT reaction solution (solution F), 1 tube, 0.1ml / tube, containing RT reaction solution (10μl system), including 5×Buffer, dNTP, DEPC-H 2 O, random primers, RNase inhibitor RNAsin (RI), reverse transcriptase M-MLV (RT). 7. RT-PCR reaction solution (solution G), 1 tube, 0.5ml / tube, containing RT-PCR reaction solution (50μl system), including 10×Buffer (including mg 2+ ), dNTP, forward primer, reverse primer, ddH 2 O and TaqE. 8. Positive control (solution H), 1 tube, 20ul / tube, containing VNN...
Embodiment 2
[0042] Embodiment 2: detection method of grouper viral neuronecrosis virus
[0043] Using the kit of Example 1, proceed as follows: 1. Take 0.1 g of the sample and add 1 ml of solution A to dilute, homogenize in an ice bath in a homogenizer, and stand at room temperature for 3 to 5 minutes. 2. Add 200 μl of solution B to the above homogenate, mix by inverting up and down, and let stand for 5 minutes. Centrifuge at 12000r / min for 15min at 3.4°C. 4. Take 400 μl supernatant, add it to 500 μl solution C, shake gently, and let stand for 10 minutes. 5.4°C, centrifuge at 12000r / min for 15min. 6. Discard the supernatant, wash twice with 1ml pre-cooled solution D, and centrifuge at 7500r / min at 4°C for 5min. 7. Air-dry or blow-dry on an ultra-clean workbench, add 50 μl E liquid water to dissolve (if it cannot be completely dissolved, it can be placed at 55-60°C for 10 minutes). The resulting RNA extract can be stored at -20°C. 8. Preheat the RNA extraction solution at 95°C for 5 m...
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