Duplex fluorescent quantitation RT-PCR (Reverse Transcription-Polymerase Chain Reaction) detection kit for shellfish Bonamia and Perkinsus
A baglamemia, double fluorescence technology, applied in the direction of recombinant DNA technology, DNA/RNA fragments, etc., can solve the problems of high requirements and complexity of reagents and primers
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Embodiment 1
[0044] Embodiment 1, design and synthesis of primers and Taqman probes
[0045] Two pairs of specific primers and two Taqman probes were designed using the Primer Express 3.0 software according to the conserved sequences of Lammia and Pijenia in GenBank (Table 1).
[0046] Table 1 is the primer and TaqMan probe sequence (5'-3')
[0047]
Embodiment 2
[0048] Embodiment 2, fluorescence quantitative RT-PCR detection
[0049] 1. Determination of fluorescent quantitative RT-PCR detection method
[0050] 1. Sample preparation
[0051] According to the instructions of the marine animal tissue genome extraction kit, extract the genomic DNA of Lammia, Monospora, Pichet, Malteia refraction, Vibrio parahaemolyticus, Vibrio alginolyticus, and Vibrio riverina.
[0052] 2. Preparation of standard products
[0053]The genomic DNA of the above-mentioned obtained Bolamia worm was used as a template for PCR amplification, and the reaction system was 50 μL (containing 25 μL PCR Mix, 1 μmol / L primers (Bonamia (760)-1 and Bonamia (760)-2, see Table 2) ), 19μLddH 2 (0, 4 μL DNA template), the reaction conditions were: 95°C pre-denaturation for 5 min, 94°C for 60 s, 52°C for 60 s, 72°C for 60 s, 35 cycles, and 72°C for 10 min. Obtain 760bp PCR product, this PCR product is cloned into pMD-18T carrier, obtains Bonamia760 plasmid; Sequencing Bo...
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