Duck Tembusu virus and Egg Drop Syndrome Virus Duplex Fluorescent Quantitative RT-PCR Detection Kit
A technology for duck Tembusu virus and egg drop syndrome, which is applied in the determination/inspection of microorganisms, recombinant DNA technology, biochemical equipment and methods, etc., can solve the problems of complexity, high requirements for reagents and primers, and achieve detection sensitivity high effect
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Embodiment 1
[0036] Embodiment 1, design and synthesis of primers and Taqman probes
[0037] According to the conserved sequences of duck Tembusu virus and egg drop syndrome virus in GenBank, multiple sets of probes and primers were designed using PrimerExpress 3.0 software, and two pairs of specific primers were selected by analyzing the dimer between the primers and two Taqmam probes (Table 1).
[0038] Table 1 is the primer and TaqMan probe sequence (5'-3')
[0039]
Embodiment 2
[0040] Embodiment 2, establishment of fluorescent quantitative RT-PCR detection
[0041] 1. Determination of fluorescent quantitative RT-PCR detection method
[0042] 1. Sample preparation
[0043] 1), nucleic acid extraction
[0044] According to the instructions of the TIANamp virus genome DNA / RNA extraction kit, extract the RNA of duck Tembusu virus, Newcastle disease virus and H9 subtype avian influenza, and extract egg drop syndrome virus, duck circovirus, goose plague virus and duck plague The DNA of the virus.
[0045] 2), reverse transcription of RNA
[0046] Duck Tembusu virus reverse transcription synthesized cDNA, specifically as follows: establish the following reverse transcription system, the total reaction volume is 20 μL) of duck Tembusu virus AV2111 RNA is 2 μL (about 20 μg), 4 μL 8mM MgCl 2 (Dalian Bioengineering Co., Ltd., catalog number: DRR0019A), 2 μL 10×PCR buffer (Dalianbao Bioengineering Co., Ltd., catalog number: DRR0019A), 2 μL 10 mM dNTP (four b...
Embodiment 3
[0076] Embodiment 3, the assembly of detection kit
[0077] According to the research results of Examples 1 and 2, a detection kit was assembled for easy use.
[0078] Solution A: PCR amplification buffer, primer 1, primer 2, probe A, primer 3, primer 4, probe B; among them, PrimeScript TM Reverse Transcriptase (Dalian Bao Biological Engineering Co., Ltd., catalog number: 2680A); Premix Ex Taq TM (Probe qPCR) (Dalian Bao Biological Engineering Co., Ltd., catalog number: RR390A); the final concentrations of primer 1, primer 2, and probe A were all 0.5 μmol / L, and the final concentrations of primer 3, primer 4, and probe B were all 0.2μmol / L;
[0079] Solution B: DTMUV+EDSV template, as a positive control;
[0080] Solution C: ddH 2 O, as a negative control.
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