Application of recombinant adenovirus containing porcine circovirus type 2 ORF2 genes as standard sample in nucleic acid amplification testing
A technology for porcine circovirus and recombinant adenovirus, which is applied in the field of animal disease detection, can solve the problems of complex preparation, inability to control the DNA extraction process, aerosol pollution, etc., and achieves clear adenovirus background, clear adenovirus background, and safe use. handy effect
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Embodiment 1
[0039] Example 1. Acquisition and Identification of Recombinant Adenovirus Containing Porcine Circovirus Type 2 ORF2 Gene
[0040] 1. Materials
[0041] The nucleic acid of porcine circovirus type 2 QD / 2014 strain and HEK293T and HEK293 cell lines are preserved by our laboratory. transfection reagent TransfectionReagent was purchased from Mirus Company; replication defective adenovirus expression system AdenoviralExpressionSystem was purchased from CellBiolabs; pMD19-T and competent cell Top10 were purchased from TaKaRa.
[0042] 2. Method
[0043] 1) Primer design
[0044] According to the PCV2 domestic isolate gene sequence (AY424401.1) published by GenBank, a pair of primers were designed using oligo7 software. It is used to amplify the complete ORF2 gene of PCV2, the fragment size is 702bp, and KpnI and HindIII restriction sites are introduced into the amplification primers. At the same time, primers and probes for PCV2 real-time fluorescent PCR detection were desi...
Embodiment 2
[0064] Example 2, Preparation and Inspection of Standard Samples of Recombinant Adenovirus Containing PCV2 ORF2 Gene
[0065] 1. Materials
[0066] The seventh generation pacAd5CMV-ORF2 was prepared by our laboratory. Trehalose was purchased from Beijing Zhongke Sanhuan Company.
[0067] 2. Method
[0068] 1) Aliquoting and freeze-drying of standard samples of recombinant adenovirus containing PCV2ORF2 gene
[0069] After repeated freeze-thawing of the 7th generation pacAd5CMV-ORF2 inoculated cells cultured in large quantities for 3 times, centrifuge at 1000g / min for 10min to remove the precipitate, add trehalose at 1% as a freeze-drying protective agent, and distribute at 0.5mL / bottle under sterile conditions. Packed in a vial and freeze-dried for 24 hours under vacuum.
[0070] 2) Uniformity inspection of standard samples
[0071] Randomly select 10 tubes of prepared standard products, extract DNA, and make a 103-fold dilution of each DNA. The established PCV2 fluoresc...
Embodiment 3
[0081] Embodiment 3, definite value and application of standard sample
[0082] 1. Materials
[0083] The freeze-dried product of the standard sample containing PCV2ORF2 gene for NAT detection of recombinant adenovirus was prepared by our laboratory; the primer probes PCV2F, PCV2R and PCV2P were synthesized by TAKARA Company. Viral DNA extraction kit was purchased from Tiangen Biological Company; dNTPs (2.5mmol / L) was purchased from TAKARA Company; TaqDNA polymerase was purchased from Promega Company.
[0084] 2. Method
[0085] 1) Determination of recombinant adenovirus standard samples containing PCV2ORF2 gene NAT (GEq / mL determination)
[0086] The value determination method is to calculate the copy number of the purified plasmid pMD19-T-ORF2 by measuring its absorbance value at 260nm and 280nm, and further serially dilute it to prepare a series of external standard products. The established PCV2 fluorescent PCR method was used to indirectly determine the copy number of ...
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