Recombination bacillary viral vector skeleton plasmid and application thereof
A technology for recombining baculovirus and backbone plasmid, applied in the field of animal genetic engineering
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Embodiment 1
[0023] Embodiment 1: Construction of the pFB-G-SFV backbone plasmid in the present invention
[0024] With pFastBac-Dual (purchased from Invitrogen Company) and pSFV1 (purchased from Invitrogen Company) shown in Figure 1 as materials, according to the flow process shown in Figure 1, construct the plasmid of the present invention, the specific steps are as follows:
[0025] 1. The pFastBac-Dua1 and pSFV1 plasmids were digested with SphI and SpeI respectively, and the large fragment containing the backbone of the baculovirus transfer vector and the nonstructural protein nsPs1-4 of SFV and the linearized pFastBac-Dua1 were respectively recovered. The two fragments were ligated to obtain the intermediate plasmid I, namely pFB-G-SFV1;
[0026] 2. Use pCI-neo as a template to amplify the HCMV IE Enhancer / Promoter element with SphI restriction sites at both ends, as shown in Figure 1, the middle fragment I;
[0027] 3. Insert the HCMV IE Enhancer / Promoter element obtained in step 2 ...
Embodiment 2
[0030] Embodiment 2: Utilize the backbone plasmid of the present invention to package the recombinant baculovirus with exogenous gene green fluorescent protein (EGFP)
[0031] 1. Construction of pFB-G-SFV-EGFP recombinant plasmid
[0032] In this example, the fluorescent reporter gene EGFP (Genebank serial number: 1377915) will be used to directly and objectively evaluate whether the modified vector obtained in the present invention can correctly express foreign genes, and compare the modified plasmid with the currently commonly used baculovirus backbone Plasmids vary in transfection efficiency and expression levels. Using plasmid pEGFP-C1 (purchased from ClonTech Company) as a template to amplify the EGFP sequence (Genebank sequence number: 1377915) with BamHI and SmalI restriction sites at both ends, insert the plasmid pFB-G- obtained in Example 1 The BamHI and SmalI restriction sites of SFV were cut to obtain the recombinant plasmid pFB-G-SFV-EGFP. The results are attache...
Embodiment 3( application Embodiment 1
[0060] The Bac-G-SFV-EGFP recombinant baculovirus packaged by the method described in Example 2 was used to infect suckling hamster kidney cells (BHK-21).
[0061] 1. In a six-well plate with 9×10 5The density inoculation number of each cell / 2ml / hole is GDC010 Syrian hamster kidney cell line BHK-21 (purchased from the commercial cell material of the Chinese Type Culture Collection Center in Wuhan University, China, see http: / / www.bio-equip.com / showlequip.asp? equipid=14757&division=2604 ) cells, cultured at 37°C for 1 h to allow the cells to adhere to the wall.
[0062] 2, with Ca 2+ , Mg 2+ Phosphate buffered saline solution (PBS, purchased from Sigama Company) was used to wash the cells three times, and the baculovirus Bac-G-SFV-EGFP was inserted into the six-well plate cells at a dose of 50 multiplicity of infection (MOI=50), 27 After infection for 4 hours at °C, the supernatant was discarded, and fresh DMEM containing 10% newborn bovine serum (purchased from Gibico) w...
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