Autoantibody joint detection ELISA kit for early screening of esophageal squamous carcinoma
An autoantibody and combined detection technology, applied in the fields of molecular biology and oncology, can solve problems such as unreported, and achieve the effects of convenient use, improved detection rate, and good technical reproducibility
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0030] Embodiment 1: the preparation of kit
[0031] 1. Experimental materials and reagents:
[0032] (1) Four kinds of tumor-associated antigen proteins (P53, TP53, CDKN2B and NPM1), purchased from Wuhan Aimeijie Technology Co., Ltd.;
[0033] (2) 96-well ELISA plate: 3590 (costar. USA);
[0034] (3) Coating solution: 50mM carbonate buffer solution, pH=9.6;
[0035] (4) Blocking solution: PBST buffer containing 2% (W / V) BSA;
[0036] (5) Sample diluent: PBST buffer containing 1% (W / V) BSA;
[0037] (6) Secondary antibody diluent: PBST buffer containing 1% (W / V) BSA;
[0038] (7) Enzyme-labeled secondary antibody: horseradish peroxidase-labeled RecA protein (Invitrogen);
[0039] (8) Washing solution: PBST (phosphate Tween) buffer containing 0.2% Tween 20;
[0040] (9) Positive control serum: P53 positive control serum, that is, the serum of patients with esophageal squamous cell carcinoma who were positive for P53 antibodies by indirect ELISA and Western blot;
[0041]...
Embodiment 2
[0066] Embodiment 2: the usage method of kit
[0067] 1. Serum sample incubation:
[0068] Dilute the serum sample to be tested with the sample diluent at a ratio of 1:500, and then add the diluted serum sample to the reaction wells of the 96-well microplate plate coated with antigen, with a sample volume of 100 μl / well, Place in a constant temperature incubator at 37°C and incubate for 1 h, then discard the liquid in the reaction well, and wash with washing solution 3 times, each time for 3 min.
[0069] 2. Enzyme-labeled secondary antibody incubation:
[0070] Dilute the horseradish peroxidase-labeled RecA protein with the secondary antibody diluent at a ratio of 1:40000, and then add the diluted horseradish peroxidase-labeled RecA protein to the reaction wells of the 96-well microtiter plate In this method, the sample volume was 100 μl / well, and incubated in a constant temperature incubator at 37°C for 50 minutes, then the liquid in the reaction well was discarded, and wa...
Embodiment 3
[0075] Embodiment 3: Analysis of the diagnostic value of the kit of the present invention
[0076] Serum samples from patients with early esophageal squamous cell carcinoma and normal people were detected using the kit described in Example 1 of the present invention to evaluate and analyze the value of the kit of the present invention for screening and diagnosis of early esophageal squamous cell carcinoma.
[0077] 1. Sample source
[0078] A total of 160 serum samples were collected from the Henan Key Open Laboratory of Esophageal Cancer, the First Affiliated Hospital of Zhengzhou University, including 80 normal human serum samples (control group) and 80 serum samples from early ESCC patients (early ESCC group). The sera of 80 normal people came from the healthy check-up population of the physical examination center of the laboratory's cooperative hospital, without any evidence of tumor-related. Among the 80 normal subjects, there were 43 males and 37 females, with an averag...
PUM
Property | Measurement | Unit |
---|---|---|
Sensitivity | aaaaa | aaaaa |
Sensitivity | 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