DNA molecule, recombinant virus and preparation method and application of DNA molecule and recombinant virus
A DNA molecule and recombinant virus technology, applied in the biological field, can solve problems such as the decline of mosquito vector control, and achieve the effect of simple method, saving time and manpower, and strong proliferation ability
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[0064] The recombinant vector can be either a recombinant cloning vector or a recombinant expression vector. According to an embodiment of the present invention, the recombinant vector may be a recombinant vector in which the DNA molecule is inserted between the multiple cloning sites (such as NotI and Xho I) of the pANCR vector (the sequence is shown in SEQ ID NO: 4). .
[0065] The transgenic cell line can be a cell containing the recombinant vector of the present invention, for example, can be obtained by transferring the recombinant vector of the present invention into cells (eg, BHK-21 cells or Vero cells).
[0066] The recombinant strain can be a strain containing the recombinant vector of the present invention, for example, it can be obtained by transforming the recombinant vector of the present invention into a competent strain (eg, Escherichia coli competent strain MC1061).
[0067] The recombinant virus of the present invention can be obtained by introducing the rec...
Embodiment 1
[0073] This example is used to illustrate the construction and identification of recombinant yellow fever virus Nluc-YF-17D.
[0074] 1. Construction of recombinant plasmid pACNR-NLuc-YF-17D
[0075] (1) The full-length infectious clone pACNR / FLYF-17Dx of the yellow fever virus vaccine strain YF-17D (gifted by Prof. Charles M. Rice of The Rockefeller University, Bredenbeek PJ, Kooi EA, Lindenbach B, Huijkman N, RiceCM, Spaan WJ .2003.A stable full-length yellow fever virus cDNA clone and therole of conserved RNA elements in flavivirus replication.The Journal ofgeneral virology 84:1261-1268.) and pNL1.1 plasmid (purchased from Premega) as templates, passed Oligo7 The software designed PCR primer sequences, amplified the Nluc gene fragment with ordinary PCR, and inserted the Nluc reporter gene into the full-length infectious clone pACNR / FLYF-17Dx of the yellow fever virus vaccine strain YF-17D by multiple fusion PCR, and constructed a Yellow fever reporter virus full-length inf...
Embodiment 2
[0117] This example is used to illustrate the use of IFA to detect the viral protein expression of recombinant yellow fever virus in BHK-21 cells. The following determinations were made to the recombinant yellow fever virus and yellow fever attenuated vaccine strain YF-17D obtained in the section "Second, the rescue of recombinant yellow fever virus Nluc-YF-17D" in Example 1:
[0118] 1. Transfer BHK-21 cells to a 6-well plate pre-placed with a coverslip, at 37°C, 5% CO 2The cells were cultured in an incubator until the cell coverage area reached about 80%, and BHK-21 cells were infected with the rescued recombinant yellow fever virus and yellow fever attenuated vaccine strains respectively. It was fixed in acetone for 30 minutes, washed with PBS and air-dried to obtain an antigen sheet, which was then stored in a -20°C refrigerator.
[0119] 2. Detect the virus-specific protein in BHK-21 cells by indirect immunofluorescence, the method is as follows: take out the antigen she...
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