Novel coronavirus antigen detection kit and preparation method thereof
A coronavirus and antigen detection technology, applied in the field of novel coronavirus antigen detection kits and their preparation, can solve the problem of slow detection speed, poor accuracy of results, and inability to meet the rapid screening of large-scale close contacts and asymptomatic infections, etc. problems, to achieve the effect of overcoming the long detection cycle
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0042] Embodiment 1: the preparation of colloidal gold solution
[0043] 1. Cleaning of glassware
[0044] The cleanliness of the glassware is directly related to the quality of the colloidal gold solution. If the utensils are not clean, the prepared colloidal gold solution will have uneven particle size, floating solids or turbidity. Immerse all the glassware required for the preparation of colloidal gold in 0.1mol / L sodium hydroxide solution for 2 hours, then rinse the glassware with purified water until neutral, then rinse the glassware with ultrapure water for three Put the rinsed utensils in an orderly manner into a blast drying oven, bake at 65°C for 8.5 hours, and put them in a clean finishing box for later use.
[0045] 2. Preparation of Colloidal Gold Solution
[0046] Colloidal gold solution was prepared by trisodium citrate reduction method; 100mL of ultrapure water was added to the conical flask, and 1.3mL of chloroauric acid solution with a mass concentration of...
Embodiment 2
[0049] Embodiment 2: Material preparation and assembly of colloidal gold kit
[0050] 1. Antibody labeling
[0051] Take 1mL of the above colloidal gold solution and place it in a 2mL EP tube, add 9μL of 0.2M potassium carbonate solution dropwise into the colloidal gold solution to adjust the pH of the solution, and then slowly and evenly add 15μg of mouse anti-SARS-Cov-2 to the solution NP monoclonal antibody 1, placed in the mixer at room temperature and mixed for 30 minutes; after mixing, quickly add 100 μL of 10% bovine serum albumin solution to the solution, placed in the mixer and continued to mix for 20 minutes, Take it out and let it stand at room temperature for 30 minutes; after standing, transfer the solution into a centrifuge and centrifuge at a speed of 13,000 rpm for 30 minutes; separate the precipitate after centrifugation, and dissolve the precipitate in 700 μL of colloidal gold resuspension buffer to obtain Resuspend the antibody in colloidal gold and store a...
Embodiment 3
[0061] Embodiment 3: Optimization of detection sample diluent
[0062] 1) Prepare different sample dilutions
[0063] Sample diluent a: configure a solution containing 0.05% Proclin300 and 0.9% sodium chloride;
[0064] Sample diluent b: prepare a solution containing 0.9% sodium chloride, 1% Tween 20 and 0.05% Proclin300;
[0065] Sample diluent c: prepare a solution of 0.01M PB containing 0.05% Proclin300 and pH7.4;
[0066] Sample diluent d: configure a solution containing 1% Tween 20, 0.05% Proclin300 and 0.01M PBS with pH7.4;
[0067] Sample diluent e: configure 0.01M PBS solution containing 0.5% Triton, 0.05% Proclin300 and pH7.4;
[0068] Sample diluent f: configure a solution containing 0.5% Triton, 0.3% EDTA and 0.01M PBS at pH 7.4;
[0069] Sample diluent g: prepare a solution containing 0.5% Triton, 0.05% SDS, 0.3% EDTA, 0.05% Proclin300 and 0.01M PBS with pH7.4.
[0070] 2) Use the sample diluent to detect and select the test card
[0071] a. First use the sam...
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