Kit for quantitatively detecting cTnT/NT-proBNP/D-dimer and application thereof
A quantitative detection and kit technology, applied in biological tests, measurement devices, material inspection products, etc., can solve the problems of single diagnosis and few simultaneous detection methods, and achieve timely and targeted treatment and improve the effect of survival rate.
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[0067] Second, the preparation method of the sample pad:
[0068] 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.
[0069] Three, the preparation method of binding pad:
[0070] The bonding pad described in the application is prepared by the following steps:
[0071] Soak the glass fiber membrane in 150mM Tris-HCL treatment solution (containing 1.0% Triton X-100, 2.5% BSA, pH7.4), soak at 4°C for 2 hours, then take it out of the oven at 37°C and dry it for 4 hours for use. The glass fiber membrane was placed on the Bio-DotXYZ3050 three-dimensional spraying platform, and the rare earth fluorescent microspheres labeled anti-cardiac troponin T, anti-N-terminal atrial natriuretic peptide, and anti-D- Dimeric antibody and goat anti-chicken IgY antibody, the obtained anti-cardiac troponin T antibody-fluorescent microsphere couplin...
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