Prawn white spot complex virogene diagnostic kit and detecting method thereof
A technology for vitiligo syndrome and genetic diagnosis, which is applied in the fields of biochemical equipment and methods, microbial determination/inspection, etc., can solve the problems of difficulty in promotion, troublesome material preparation, and low sensitivity, so as to improve the efficiency of scientific management and avoid the spread of viruses. Popular, fast-paced effects
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Embodiment 1
[0040] Embodiment 1: the genetic diagnosis kit of prawn white spot syndrome virus
[0041] The kit consists of the following components (10 samples):
[0042] 1. Sample diluent (solution A), 1 tube, 5ml / tube, filled with phosphate buffer (1×PBS), pH7.4.
[0043] 2. Template extraction solution (solution B), 1 tube, 10 μl / tube, containing proteinase K.
[0044] 3. PCR reaction solution (solution C), 1 tube, 250μl / tube, containing PCR first expansion reaction solution (25μl system), including ddH 2 O, 10×Buffer (including mg 2+ ), dNTP, outer primer F1, outer primer R1 and TaqE.
[0045] 4. PCR reaction solution (solution D), 1 tube, 250μl / tube, containing PCR secondary amplification reaction solution (25μl system), including ddH 2 O, 10×Buffer (including mg 2+ ), dNTP, inner primer F2, inner primer R2 and TaqE.
[0046] 5. Positive control (solution E), 1 tube, 20 μl / tube, containing WSSV positive DNA.
[0047] 6. Cuboid box, 8.5×5.8×6.2cm 3 .
[0048] 7. A piece of fo...
Embodiment 2
[0069] Embodiment 2: the detection method of prawn white spot syndrome virus
[0070] Use the test kit of embodiment 1, carry out according to the following steps:
[0071] 1. Take 0.05 g of the sample to be tested, add 500 μl of sample diluent (solution A) to dilute 10 times, and homogenize in an ice bath in a homogenizer.
[0072] 2. Centrifuge at 6000r / min for 5min.
[0073] 3. Take 50 μl supernatant and add 1 μl template extract solution (solution B), boil for 15 minutes, and immediately put it on ice for 5 minutes.
[0074] 4. Centrifuge at 8000r / min for 10min, and use the supernatant as a PCR template.
[0075] 5. Take 2 μl of the template and solution E respectively, add them to the PCR reaction solution (solution C), mix well, centrifuge for a few seconds, and place on the PCR instrument.
[0076] 6. Amplify according to the following conditions:
[0077] Pre-denaturation at 95°C for 2min → 34 cycles at 94°C for 45sec → 10min at 72°C → storage at 4°C
[0078] ...
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