Family-planning four-item combined kit employing enzyme linked immunosorbent spot assay
An enzyme-linked immunospot and kit technology, applied in the direction of measuring devices, instruments, scientific instruments, etc., can solve the problems of inconvenient portability and operation, no spot reaction plate, complicated detection process, etc., to achieve easy popularization and novel design , the effect of simple operation
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Embodiment 1
[0020] Such as figure 1 As shown, the present invention is provided with a carrier plate 1, a nitrocellulose membrane 2 pasted on the surface of the carrier plate 1, a cytomegalovirus antibody (antigen) detection point 3, a toxoplasma antibody (antigen) detection point 4, a rubella virus antibody (antigen) detection point ) detection points 5, herpes simplex virus antibody (antigen) detection points 6, and control points 7 are sequentially arranged on the nitrocellulose membrane 2 from top to bottom, and incubation tanks 8 are formed around each detection line point and control point; Corresponding antigens ( antibody); at control point 7, there are four control points 9-12 from left to right, respectively coated with cytomegalovirus antigen, toxoplasma gondii antigen, rubella virus antigen, herpes simplex virus antigen or coated with cytomegalovirus antibody , Toxoplasma gondii antibody, rubella virus antibody, herpes simplex virus antibody positive serum.
[0021] Such as ...
Embodiment 2
[0031] Example 2, the method of using the four combined kits of enzyme-linked immunospot family planning of the present invention
[0032] 1. The sample to be tested is diluted 1:50 with 0.01mol / L PBS buffer.
[0033] 2. Take out the carrier plate, pipette 0.2mL-0.3mL of the sample to be tested, put it into the incubation tank, and incubate at room temperature (18-25)°C for 30min.
[0034] 3. Aspirate the liquid in the incubation tank, wash each incubation tank with 2mL 0.01mol / L PBS buffer solution 3 times, 5min each time.
[0035]4. Add enzyme conjugates: Add 0.2mL-0.3mL enzyme conjugates (use alkaline phosphatase-labeled secondary antibody (corresponding antibody) or horseradish peroxidase-labeled secondary antibody (corresponding antibody) into the incubation tank respectively antibody)), incubate at 18-25°C for 30min.
[0036] 5. Aspirate the liquid in the tank, wash each incubation tank with 2mL0.01mol / L PBS buffer solution 3 times, 5min each time.
[0037] 6. Substra...
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