Chronic kidney disease marker suPAR detection kit and preparation method thereof
A chronic kidney disease and detection kit technology, applied in the field of medical products, can solve the problems of complex operation and lack of research on chronic kidney disease, and achieve the effects of simple operation, convenient measurement, high accuracy and specificity
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Embodiment 1
[0016] Example 1 Preparation of dry immunofluorescence kit for chronic kidney disease suPAR of the present invention
[0017] The kit of the present invention comprises a PVC base plate, a fluorescent binding pad, a nitrocellulose membrane, a sample pad and a water-absorbing pad; the sample pad, the nitrocellulose membrane, the fluorescent binding pad, and the water-absorbing pad are fixed on the PVC base plate in a horizontal direction.
[0018] 1. Preparation of nitrocellulose membrane (NC membrane)-PVC bottom plate
[0019] 1. Scribing film: Cut the nitrocellulose into 25mm×300mm and paste it on the PVC bottom plate. Dilute the rabbit anti-chicken IgY with PBS to a concentration of 1 mg / ml as the C-line coating solution; dilute the mouse anti-human SUPAR monoclonal antibody 2 with PBS to a concentration of 1 mg / ml as the T-line. Using a film sprayer, streak the T-line coating solution and C-line coating solution on the nitrocellulose membrane to obtain the test line and qu...
Embodiment 2
[0028] Embodiment 2 The usage method of kit of the present invention
[0029] 1. Use a pipette to pipette 50ul serum, plasma, and cerebrospinal fluid samples and add them to the sample pad of the test strip;
[0030] 2. Stand at room temperature for 10 minutes;
[0031] 3. At the end of 10 minutes, put the test strip into the immunofluorescence quantitative analyzer to read the data;
[0032] 4. The immunofluorescence quantitative analyzer measures and analyzes the optical signal, and quantitatively obtains the concentration of the tested substance;
[0033] 5. Judgment of negative and positive according to the reference value.
Embodiment 3
[0034] Embodiment 3 Comparison between the kit of the present invention and the ELISA kit
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