Kit and method for achieving highly-sensitive multiterm joint inspection of allergen-specific IgE antibodies
An allergen and kit technology, which is applied to the kits and fields of highly sensitive multiple joint detection of allergen-specific IgE antibodies, to achieve the effect of less sample consumption and lower dosage
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0018] Provided is a high-sensitivity kit for multiple joint detection of allergen-specific IgE antibodies, including a membrane strip, a polymerase-coupled anti-human IgE antibody, and a substrate chromogen matching the polymerase-coupled anti-human IgE antibody. The film strip is a fibrous material film cured with str-bio-allergen. The polymerase-coupled anti-human IgE antibody is commercially available, and used to prepare a working solution with a concentration of 1:100-10,000 with PBS containing 0.05% TritonX-100 at a pH of 7.4. The substrate chromogenic reagent corresponding to the anti-human IgE antibody coupled to the polymerase is commercially available or can be prepared by itself. The anti-human IgE antibody is goat anti-human IgE antibody, rabbit anti-human IgE antibody or mouse anti-human IgE antibody, and the polymerase is poly-alkaline phosphatase or poly-horseradish peroxidase. The above are the main components of the reagents, excluding conventional reagents ...
Embodiment 2
[0036] Provide a highly sensitive multiple joint detection method for allergen-specific IgE antibody detection, including the following steps:
[0037] (1) Place the antigen membrane strip in the incubation tank, please put the side with the text mark up; add 1ml of sample buffer (50mMPH7.4 Tris buffer) to each tank, and shake the membrane strip slightly at room temperature for 5 minutes, then suck it off.
[0038] (2) Add 1ml of diluted serum sample to each tank (use the sample diluent to half-dilute the serum sample), and incubate for 30 minutes at room temperature on a rocking shaker.
[0039] (3) Suck off the liquid in the incubation tank. Then, add 1ml of washing buffer (0.05% Tween 20, 50mMPH7.4 Tris buffer, 0.05% sodium azide) to each tank, shake gently on a rocking table at room temperature for 5 minutes, and suck off the liquid in the incubation tank. Repeat the wash 2 more times.
[0040] (4) Suck off the liquid in the incubation tank. Add 1ml of enzyme conjugate...
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