Hybridoma cell strain secreting anti-amantadine monoclonal antibody and application of hybridoma cell strain
A hybridoma cell line and monoclonal antibody technology, applied in the biological field, can solve problems such as hybridoma cell lines that cannot secrete anti-amantadine monoclonal antibody, and achieve accurate immune detection and immune analysis, immune titer High, specific effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0029] The preparation of embodiment 1 hybridoma cell line
[0030] (1) Immunization of mice
[0031] Select 8-week-old BALB / c female mice to mix 10 μg of amantadine artificial antigen and quick antibody-5w adjuvant in equal volumes to form 100 μl, and inject the rear calf muscle of the mouse; the rear calf muscle part is exposed to the mouse leg Where there is a large muscle on the outside, and most of the mouse's thighs are covered by the abdominal skin, the knee joints can also be found to distinguish the calf from the thigh; two weeks later, the second injection was injected in the same way; two weeks later, intraperitoneal injection was performed with 10 μg of antigen injection.
[0032] The molecular structural formula of amantadine artificial antigen is shown in formula (I):
[0033]
[0034] In formula (I), BGG is bovine gamma globulin.
[0035] (2) Preparation of lymphocytes
[0036] Get the spleen of the BALB / c female mouse treated through step (1), grind the ...
Embodiment 2
[0064] Example 2 Reactivity test of anti-amantadine monoclonal antibody
[0065] The reactivity of the anti-amantadine monoclonal antibody prepared in Example 1 was detected by an indirect ELISA method, and the detection steps included: ① Dilute the amantadine artificial antigen to 500 ng / mL with a carbonate buffer solution with a pH of 9.6 and a concentration of 0.05M , then add 100 μl / well diluted amantadine artificial antigen to the 96-well ELISA plate, and coat overnight at 4°C;
[0066] ②Wash the plate 3 times with PBS buffer containing 0.05% tween20; then add 100 μl anti-amantadine monoclonal antibody solution with a concentration of 0.3 μg / ml, make a 1:3 dilution, and set up a negative control at the same time, react at 37 ° C for 60 minutes Afterwards, wash the plate once with PBS buffer containing 0.05% tween20;
[0067] ③ Add PBS buffer to goat anti-mouse IgG-HRP and dilute to 5000 times the volume, then add 100 μl / well diluted goat anti-mouse IgG-HRP to a 96-well c...
Embodiment 3
[0072] Such as figure 1 As shown, a kind of amantadine colloidal gold detection test strip of the present embodiment comprises sample pad, colloidal gold pad, nitrocellulose membrane and water absorption pad; Sample pad, colloidal gold pad, nitrocellulose membrane and water absorption pad are sequentially head to tail Lap on the base plate. Wherein, the colloidal gold pad is coated with the anti-amantadine monoclonal antibody prepared in Example 1 labeled with colloidal gold, and the detection line (T) of the nitrocellulose membrane is coated with the amantadine-bovine serum albumin complex, The quality control line (C) is coated with goat anti-mouse IgG. The coating amount of amantadine-bovine serum albumin complex is the detection limit of amantadine by the anti-amantadine monoclonal antibody (take 20 μg / kg as an example). The preparation method of the test strip is a conventional method in the art.
[0073] When testing, insert one end of the test strip sample pad into t...
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