GFP (Green Fluorescent Protein) tracing system of vaccinia virus and application of GFP tracing system
A technology of vaccinia virus and vaccinia virus vector, which is applied in the direction of application, virus/phage, and the use of vectors to introduce foreign genetic material, etc., to achieve the effect of stable fluorescence quality and improved virus monitoring sensitivity
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0056] Embodiment 1, construction and identification of GFP-labeled recombinant vaccinia virus
[0057] 1. Construction and identification of homologous recombination plasmids
[0058] 1. Construction and identification of recombinant plasmid pGPT-IN
[0059] No. 80267-80725 (corresponding to No. 1-459 of Sequence 1) of the genomic DNA sequence of wild-type vaccinia virus WR strain (GenBank number: NC_006998.1, Up date: 2012-11-22) was named upstream homolog Arm) and positions 80726-81194 (corresponding to positions 460-928 of sequence 1, named downstream homology arms) were cloned into the upstream and downstream of the gpt gene of plasmid pSV2-gpt, respectively, to obtain the recombinant plasmid pGPT-IN. The specific operation is as follows:
[0060] (1) Extraction of genomic DNA of wild-type vaccinia virus WR strain
[0061] The specific operation is as follows:
[0062] The wild-type vaccinia virus WR strain was appropriately diluted with DMEM complete medium, added to...
Embodiment 2
[0166] Example 2, Detection of Biological Activity of Recombinant Vaccinia Virus V.V.-GFP
[0167] 1. Determination of one-step growth curve of recombinant vaccinia virus V.V.-GFP
[0168]Infect (MOI=1) CV-1 cells with the V.V.-GFP recombinant virus prepared in Example 1. After adsorption at 37°C for 1 hour, the virus liquid was removed, and the cells were washed with DMEM for 3 times to remove residual uninfected virus. Cells were cultured at 37°C with DMEM containing 10% (volume percent) FBS. The virus was collected at different time points (0, 2, 4, 6, 8, 10, 12, 24 hours) within 0-24 hours after infection, and the collected virus was subjected to plaque analysis at 37°C to determine the virus titer (PFU / ml ), and then draw a one-step growth curve. At the same time, wild-type V.V.-WR was used as a control in the experiment to detect the difference between the V.V.-GFP recombinant virus and its one-step growth curve. Experiments were repeated three times.
[0169] The re...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com