Mandarin fish infectious splenorenal necrosis virogene diagnostic kit and detecting method thereof
A spleen and kidney necrosis virus and genetic diagnosis technology, applied in the direction of biochemical equipment and methods, microbial measurement/inspection, etc., can solve problems such as difficult promotion, troublesome material preparation, limited application and development, etc., to improve scientific management efficiency, The effect of avoiding the spread of viruses and high practical value
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Embodiment 1
[0044] Embodiment 1: the genetic diagnosis kit of mandarin fish infectious spleen and kidney necrosis virus
[0045] The kit consists of the following components (10 samples);
[0046] 1. Release solution (solution A), 2 tubes, 5ml / tube, filled with phosphate buffer solution (1×PBS), pH7.4.
[0047] 2. Template extract solution (solution B), self-prepared or prepared, phenol / chloroform / isoamyl alcohol, the ratio is 25:24:1.
[0048] 3. Solution C, 1 tube, 200μl / tube, filled with 5M NaCl.
[0049] 4. Liquid D, self-prepared, 1ml / part×10parts, 10ml, mainly absolute ethanol.
[0050] 5. E liquid, self-prepared, mainly 70% ethanol.
[0051] 6. Solution F, 1 tube, 30μl / part x 10 parts, 300μl / tube, filled with sterilized double distilled water.
[0052] 7. PCR reaction solution (solution G), 1 tube, 25μl / part × 10 copies, 250μl / tube, containing PCR first expansion reaction solution (25μl system), including ddH 2 O, 10×Buffer (including mg 2+ ), dNTP, outer primer F1, outer pri...
Embodiment 2
[0077] Embodiment 2: detection method of mandarin fish infectious spleen and kidney necrosis virus
[0078] Use the test kit of embodiment 1, carry out according to the following steps:
[0079] 1. Add 0.1 g of the sample to be tested, add 1 ml of sample diluent (solution A) to dilute 10 times, and homogenize in an ice bath in a homogenizer.
[0080] 2. Centrifuge at 4000r / min for 10min.
[0081] 3. Take 600 μl of supernatant / extract with template extract solution (solution B), invert up and down several times and mix well.
[0082] 4. Centrifuge at 12000r / min for 10min.
[0083] 5. Take 500ul supernatant and add 20μl / C solution, then add 1ml D solution, and precipitate at -20℃ for 1 hour.
[0084] 6. Centrifuge at 12000r / min for 10min.
[0085] 7. Discard the supernatant, add E solution to wash, centrifuge at 12000r / min for 5min, and wash twice.
[0086] 8. Discard the supernatant and dry it naturally or on a clean bench.
[0087] 9. Add 20-30 μl F solution to resuspend...
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