Immunochromatographic test strip for rapidly detecting acute pancreatitis and preparation method thereof
An acute pancreatitis and immunochromatography technology, applied in the field of medical testing, can solve the problems of complex colloidal gold labeling preparation process, sensitivity to be improved, and high cost, and achieve easy-to-read results, improved sensitivity and simplicity, and easy operation Effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0037] Such as figure 1 As shown, it is a structural schematic diagram of a quick detection test strip of acute pancreatitis immunochromatography according to the present invention. It is formed by lapping and pasting on the substrate 1 in sequence, and the glass fiber membrane marking pad 3 is coated with a biotin-avidin-color latex complex-labeled trypsinogen-2 high-specificity monoclonal antibody, nitric acid The cellulose-coated membrane 4 includes a detection zone 6 and a control zone 7, the detection zone 6 is coated with another trypsinogen-2 specific monoclonal antibody with a different epitope from the monoclonal antibody labeled on the glass fiber membrane marker pad 3 , the control region 7 was coated with anti-mouse antibody.
[0038] In this embodiment, the ratio of biotin:avidin:color latex is 1:1:1~2:2:3, and trypsinogen-2 labeled with biotin-avidin-color latex complex is highly specific The amount of the monoclonal antibody sprayed on the glass fiber membrane...
Embodiment 2
[0053] The detection test strip structure in this embodiment is all identical with embodiment 1.
[0054] In this embodiment, the ratio of biotin:avidin:color latex is 1:1:1~2:2:3, and trypsinogen-2 labeled with biotin-avidin-color latex complex is highly specific The amount of the monoclonal antibody sprayed on the glass fiber membrane marker pad was 35 μl / cm. The concentration of trypsinogen-2 specific monoclonal antibody on the nitrocellulose-coated membrane is 7 μg / ml, and the consumption in the detection zone is 20 μl / 35cm; the concentration of the anti-mouse antibody is 7 μg / ml, in the The amount used in the control area was 20 μl / 35cm.
[0055] In the preparation method of this example, except that the weight ratio of avidin to colored latex in step B is 2:1, and the volume ratio of biotin-labeled antibody to avidin-colored latex complex in step D is 7:1, the rest All are identical with embodiment 1, and using method is also identical with embodiment 1.
Embodiment 3
[0057] The detection test strip structure in this embodiment is all identical with embodiment 1.
[0058] In this example, the ratio of biotin:avidin:color latex is 1:1:1~2:2:3, and trypsinogen-2 labeled with biotin-avidin-color latex complex is highly specific The amount of the monoclonal antibody sprayed on the glass fiber membrane marker pad was 48 μl / cm. The concentration of trypsinogen-2 specific monoclonal antibody on the nitrocellulose-coated membrane is 13 μg / ml, and the consumption in the detection area is 20 μl / 35cm; the concentration of the anti-mouse antibody is 13 μg / ml, and the The amount used in the control area was 20 μl / 35cm.
[0059] In the preparation method of this example, except that the weight ratio of avidin to colored latex in step B is 3:1, and the volume ratio of biotin-labeled antibody to avidin-colored latex complex in step D is 10:1, the rest All are identical with embodiment 1, and using method is also identical with embodiment 1.
[0060] The...
PUM
Property | Measurement | Unit |
---|---|---|
diameter | 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