Serum amyloid A testing kit and manufacturing method
A technology of serum amyloid and kit, which is applied in the field of membrane chromatography technology, protein cross-linking technology, serum amyloid A assay kit, and marker immunoassay technology. It can solve the problems of high intensity and strong interference and achieve rapid response. , high sensitivity and strong specificity
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Embodiment 1
[0042] Each component of the test paper card in the serum amyloid A assay kit can be prepared by the following measures:
[0043] 1. Preparation of sample pad 2:
[0044] Soak the glass fiber membrane in the treatment solution containing 1.0% Triton X-100, 2.5% BSA, 0.15M Tris buffer, pH7.5, soak at 4°C for 4 hours, then place it in an oven and dry it at 37°C 2 hours.
[0045] 2. Preparation of binding pad 3 for absorbing fluorescent microsphere-labeled antibody:
[0046] Soak the glass fiber membrane in 150mM Tris-HCL treatment solution (containing 1.0% Triton X-100, 2.5% BSA, pH7.4), soak for 2 hours at 4°C, then take it out of the oven at 37°C and dry it for 4 hours, and set aside. The glass fiber membrane was placed on the Bio-DotXYZ3050 three-dimensional spraying platform, and the rare earth Eu 3+ The anti-serum amyloid A monoclonal antibody-conjugated complex labeled with fluorescent microspheres is sprayed onto a glass fiber membrane, and dried at 37°C for 1 hour.
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Embodiment 2
[0055] Embodiment 2: accuracy test
[0056] Select the above test paper card and fluorescence immunochromatography analyzer (model: NEO-007),
[0057] Setting of the parameters of the fluorescence immunoassay analyzer: After setting the process parameters of the test paper card on the fluorescence immunoassay The serum amyloid A calibrator is measured with a test paper card to obtain the fluorescence intensity value of each calibrator, and the result is input into the parameters of the analyzer to complete the setting of the parameters of the analyzer.
[0058] Main testing materials: clinical samples obtained from relevant hospitals, a total of 300 latex-enhanced immunoturbidimetric value samples, including 100 serum samples, 100 plasma samples, 100 whole blood samples, and the serum amyloid A content distribution interval is 5.00 Between -200mg / L.
[0059] Detection method:
[0060] Step 1: Equilibrate the detection reagent and sample to room temperature, take out the tes...
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