Fast chemiluminescence immune detection system and analysis method
A chemiluminescence immunoassay and detection system technology, applied in the field of rapid chemiluminescence immunoassay, can solve the problems of slow temperature rise, limitation of rapid and low-cost immunoassay method development, and increased cost, so as to improve reproducibility and reduce analysis cost , the effect of less manual operation
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Embodiment 1
[0033] Embodiment 1 The rapid chemiluminescence detection system is further described in conjunction with accompanying drawing 1:
[0034] The system consists of a solution transmission system, an incubation system, a magnetic separation system, and a signal acquisition system. Wherein the solution transmission system is composed of small test tubes (1-4), multi-position valve (5), peristaltic pump (6) and silicon rubber tube (7). The small test tube (1) is equipped with the sample to be tested, the enzyme-labeled antibody and the magnetic bead mixture with the capture antibody immobilized on the surface, and the small test tube (2) is filled with 0.01M phosphate washing buffer (pH 7.4, containing 0.05% Tween- 20), the small test tube (3) is equipped with chemiluminescent substrate solution (luminol, hydrogen peroxide and p-iodophenol), and the small test tube (4) is equipped with 0.1M hydrochloric acid solution. The four small test tubes are respectively connected to the fou...
Embodiment 2
[0035] Example 2 Rapid Chemiluminescent Immunoassay Method
[0036] The specific analysis process is shown in Table 1.
[0037]
[0038] All analysis steps are programmed and automatically controlled by computer, and the measured chemiluminescent signal is output from the computer. After the analysis steps were completed, the magnetic beads immobilized with antibodies were collected uniformly, soaked in glycine / hydrochloric acid buffer solution with pH 2.2 for 10 minutes, and washed with 0.01M phosphate buffer solution (pH 7.4) for reuse.
Embodiment 3
[0040] Taking alpha-fetoprotein (AFP), a marker with significant significance in the clinical diagnosis of tumors, as an example, the application of this automatic sample injection resolution chemiluminescence multicomponent immunoassay method is illustrated.
[0041] Using epoxy-activated magnetic beads as the carrier of the immune reaction, the mouse monoclonal AFP antibody was covalently immobilized, and the residual active sites were blocked with bovine serum albumin. The tracer antibody was goat polyclonal AFP antibody labeled with horseradish peroxidase.
[0042] As shown in the process shown in Table 1, the tumor marker AFP in clinical serum samples is used as the detection object, and a rapid chemiluminescence immunoassay is performed to obtain the concentration of AFP in the sample to be tested, which provides a method for rapid clinical screening and diagnosis. feasible method.
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