Substrate regional band resolution chemical luminescent multi-component immunity analytical method and detection system thereof
A detection system, chemiluminescence technology, applied in the direction of chemiluminescence/bioluminescence, analysis by causing chemical reaction of materials, analysis of materials, etc., can solve problems such as expensive instruments and supporting kits, and financially insufficient institutions cannot afford it , to achieve the effect of saving coating antibody, less manual operation, and simple equipment
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Embodiment 1
[0040] Embodiment 1 is combined with attached figure 1 Further description of the flow-through two-component chemiluminescence immunoassay detection system:
[0041] The flow-through substrate zone resolution multi-component chemiluminescence immunoassay detection system includes a solution delivery system, an immunoreactor, a chemiluminescence detector and a computer. The solution transmission system consists of a multi-channel peristaltic pump 6, a PTFE connecting pipe 7 with an inner diameter of 0.8mm and a multi-position selector valve 8. The five connecting pipes 7 are respectively connected to the multi-position selector valve through the multi-channel peristaltic pump 6. The five valve positions of valve 8 are ports 1, 2, 4, and 5. Inlet 1 transfers sample S, inlet 5 transfers regeneration buffer RB, inlet 4 transfers washing buffer WB, and inlets 3 and 2 transfer two chemiluminescent substrates respectively S 1 and S 2 One end of each connecting pipe 7 is connected ...
Embodiment 2
[0042] Embodiment 2 chemiluminescence and component immunoassay method:
[0043] Table 1 Specific analysis process
Embodiment 3
[0045] Taking two important tumor markers: carcinoembryonic antigen (CEA) and cancer antigen 125 (CA 125) as examples, the application of the flow-type two-component chemiluminescence immunoassay system is illustrated.
[0046] The immunoreactor is an aldehyde-activated UltraBind membrane coated with mouse monoclonal anti-CEA and mouse monoclonal anti-CA 125. The remaining active sites are blocked with bovine serum albumin and fixed in a 50 microliter flow cell. The tracer antibody to CEA was mouse monoclonal anti-CEA labeled with alkaline phosphatase, and the tracer antibody to CA 125 was mouse monoclonal anti-CA 125 labeled with horseradish peroxidase.
[0047] As shown in Table 1, the valve is switched to position 1, and the mixture of 25 microliters of sample, 12.5 microliters of CEA tracer antibody and 12.5 microliters of CA 125 tracer antibody is passed into the flow cell where the immunoreactor is fixed, Incubate statically for 20 minutes. Then switch the valve positio...
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