Duck Flavovirus and Duck Plague Virus Duplex RT-PCR Detection Kit
A technology of RT-PCR and detection kits, which is applied in the direction of recombinant DNA technology, measurement/testing of microorganisms, DNA/RNA fragments, etc., and can solve complex problems
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Embodiment 1
[0032] Embodiment 1, design and synthesis of primers
[0033] According to the conserved sequences of the E gene of BYD and the UL6 gene of DPV in GenBank, DNAStar software was used for multiple sequence alignment, and primer5.0 was used to design primers in the conserved regions. Primers were synthesized by Beijing Liuhe Huada Gene Technology Co., Ltd. (Table 1).
[0034]Table 1 Primer Information
[0035]
Embodiment 2
[0036] Embodiment 2, establishment of double RT-PCR detection method
[0037] 1. Extraction of nucleic acid and reverse transcription of RNA
[0038] According to the instructions of the DNA / RNA extraction kit, extract the DNA of duck plague virus, Muscovy duck parvovirus, duck circovirus and egg drop syndrome virus; simultaneously extract duck yellow virus, duck hepatitis virus, H9 subtype avian influenza virus, The RNA of duck-derived Newcastle disease virus was reverse-transcribed into cDNA according to the reverse transcription instructions, as follows: the following reverse transcription system was established, with a total reaction volume of 20 μL, and the above viral RNA was reverse-transcribed according to the reverse transcription instructions (Beijing Quanshi Jin , AT301-02), 8 μL of RNA, 1 μL of random primers, 10 μL of 2×TSReactionMix, 1 μL of TransScriptRT / RIEnzymeMix, 10 min at 25 °C, 30 min at 42 °C, 5 min at 85 °C, and end at 4 °C to obtain duck yellow virus, d...
Embodiment 3
[0049] Embodiment 3, the assembly of detection kit
[0050] According to the research results of Examples 1 and 2, a detection kit was assembled for easy use.
[0051] Solution A: PCR reaction solution, containing 12.5 μL of 2×TaqPCRMix (Beijing Quanshijin, AS111-12), 0.5 μL of BYD upstream and downstream primers (both primer concentrations are 50 μmol / mL, and the final concentration in the reaction system is 1 μmol) / mL), 0.5 μL each of DPV upstream and downstream primers (primer concentration is 50 μmol / mL, and the final concentration in the reaction system is 1 μmol / mL), add ddH 2 O8.5 μL.
[0052] Solution B: Contain 1 μL each of BYD+DPV template as a positive control.
[0053] Solution C: Contains ddH 2 O1μL, as a negative control.
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