Hybridoma cells, monoclonal antibodies capable of secreting anti-type II dengue virus ns1 monoclonal antibodies and their applications
A monoclonal antibody, dengue virus technology, applied in the field of immune detection, can solve the problem of not being able to meet the needs of clinical diagnosis well, and achieve the effect of high secretion yield
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0032] Establishment of hybridoma cells and preparation of anti-type II dengue virus NS1 monoclonal antibody.
[0033] 1. Preparation of immunogen.
[0034] Recombinant type II dengue virus NS1 protein expressed by insect cells (sf9 cells and High Five cells in this example) was used as an immunogen. The NS1 gene of type II dengue virus (Shanghai Sangon Bioengineering Co., Ltd.) and the genome of baculovirus (purchased from Shanghai Yingjun Biotechnology Co., Ltd.) were subjected to homologous recombination to construct a dengue virus carrying NS1 gene of type II. Baculovirus, and then by transfecting sf9 cells (purchased from Shanghai Yingjun Biotechnology Co., Ltd., preserved by the company), a large amount of recombinant baculovirus was amplified, and the amplified recombinant baculovirus was infected with High Five cells ( Purchased from Shanghai Yingjun Biotechnology Co., Ltd. and preserved by our company), the target NS1 protein is efficiently secreted and expressed by ...
Embodiment 2
[0075] Preparation of colloidal gold test paper for detection of type II dengue virus NS1 antigen.
[0076] 1. Preparation of nitrocellulose membrane
[0077] Preparation of coating buffer: 6% methanol, 0.01M pH7.2 PBS buffer as coating buffer, filtered through 0.22 μm membrane, set at 4°C for later use, valid for one week. 1000ml 6% methanol 0.01M pH 7.2PBS buffer formulation: NaCL 8g, KCL 0.2g, NaCl 2 HPO 4 12H 2 O 2.9g, KH 2 PO 4 0.2g, methanol 60ml, distilled deionized water to 1000ml.
[0078] Preparation of nitrocellulose membrane: Dilute the monoclonal antibody DN2-9 prepared in Example 1 to 1-5 mg / ml with coating buffer, adjust the machine, draw the T line, which is the detection line, and the T line is close to The pad end of the gold label is about 5mm away from the pad end of the gold label; dilute the goat anti-mouse IgG antibody (manufactured by Shenzhen Feipeng Biological Co., Ltd., product number BA-PAB-MU0001) to 1-5mg / ml with coating buffer, Adjust the ...
Embodiment 3
[0103] A kit for detecting the NS1 protein of dengue virus type II.
[0104] 1. The kit for rapid detection of type II dengue virus NS1 protein comprises: the detection test paper and sample diluent prepared in Example 2.
[0105] The sample diluent was 8% NaCl solution. Preparation method: 80gNaCl, add distilled water to make up to 1000ml.
[0106] 2. Detection of type II dengue virus NS1 protein by colloidal gold method.
[0107] (1) Directly pipette 120 μl of collected human serum or plasma into the sample hole of the test paper card, and wait for 15 minutes to observe the results.
[0108] (2) Judgment of results: When the test strip shows a red quality control line visible to the naked eye, but no red detection line visible to the naked eye, the result is judged as negative; when the test strip shows a red quality control line visible to the naked eye, it also appears Visible red test line, the result is judged as positive. The darker the detection line, the higher th...
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