Duck hepatitis virus polyprotein antigen sense region DHAV-Mag genetic recombination protein and preparation method and application thereof
A duck hepatitis virus and polyprotein technology, applied in the field of biomedicine, can solve the problem of whether the capsid protein is completely cleaved and the quantity cannot be confirmed, and achieves the effects of good reactogenicity, low preparation cost and strong specificity
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0054] A duck hepatitis virus polyprotein antigen-dense region DHAV-MAg gene recombinant protein, its amino acid sequence is shown in SEQ ID NO: 1, and its DNA sequence is shown in SEQ ID NO: 2.
[0055] A method for preparing recombinant protein of duck hepatitis virus polyprotein antigen dense region DHAV-MAg gene, comprising the steps of:
[0056] Step 1: DHAV-MAg gene DNA fragment cloning in the polyprotein antigen-dense region of duck hepatitis virus: analysis and determination of the DHAV-MAg gene and restriction sites in the polyprotein antigen-dense region of duck hepatitis virus, according to Genbank accession number JQ316452.1 The whole gene sequence of DHAV-1X strain, the design of specific primers to amplify the DHAV-MAg gene DNA fragment in the polyprotein antigen-dense region of duck hepatitis virus, and the addition of BamHI and XhoI restriction enzymes to the 5' ends of the upstream and downstream primers site, extract duck hepatitis virus RNA, use specific pri...
Embodiment 2
[0103] The expression condition optimization of embodiment 2DHAV-MAg gene recombinant protein
[0104] experimental method:
[0105] 1. Optimization of IPTG concentration
[0106] Inoculate the expressing bacteria into four LB / Amp medium test tubes at a ratio of 1:100, and culture at 37°C until OD 600nm At 0.6, add IPTG to the final concentration: 0mmol / L, 0.4mmol / L, 0.8mmol / L and 1.2mmol / L to induce culture for about 4h, sample treatment, SDS-PAGE electrophoresis.
[0107] 2. Optimization of induction time
[0108] Inoculate the expressing bacteria into 6 LB / Amp medium test tubes according to the ratio of 1:100, and wait until OD 600nm After reaching 0.6, add the optimal IPTG concentration, induce 4h, 6h, 8h, 10h, 12h and no induction respectively, the treatment is the same as above.
[0109] 3. Optimization of induction temperature
[0110] Inoculate the expressing bacteria into 3 LB / Amp medium test tubes at a ratio of 1:100, and wait until OD 600nm After reaching 0.6,...
Embodiment 3
[0113] Example 3 Activity Analysis of DHAV-MAg Gene Recombinant Protein and Preparation, Characteristics and Application of Hyperimmune Serum
[0114] experimental method:
[0115] 1. Preparation of rabbit anti-DHAV-MAg gene recombinant protein hyperimmune serum
[0116] Immunogen preparation: prokaryotic expression of DHAV-MAg gene recombinant protein and purification of DHAV-MAg gene recombinant protein with high purity, stored at -20°C for future use.
[0117] Animal immunization protocol:
[0118] Select young healthy rabbits with appropriate body weight and carry out immunization according to Table 1.
[0119] Table 1 The immune program for the preparation of rabbit anti-DHAV-MAg gene recombinant protein hyperimmune serum
[0120]
[0121] Serum collection and determination of rabbit antiserum titer: 7 days after the last immunization, blood was collected, kept at 37°C for 2 hours, and refrigerated overnight at 4°C after coagulation. Serum was collected, tested for...
PUM
Property | Measurement | Unit |
---|---|---|
diameter | aaaaa | aaaaa |
concentration | aaaaa | aaaaa |
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