Immunochromatographic test strip for semi-quantitatively and simultaneously detecting cTnI and Myo and preparation method thereof
An immunochromatographic test paper, semi-quantitative technology, applied in biological testing, analytical materials, measuring devices, etc., can solve the problems of narrow linear range and low sensitivity of polyproteins, and achieve good specificity, high sensitivity, and good application prospects Effect
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Embodiment 1
[0030] 1) Soak the sample pad in the sample pad treatment solution for 30 minutes, take it out and dry it in a 37°C drying oven for 12 hours, then add a desiccant and store it for later use; the sample pad treatment solution contains 1% BSA, 0.05% Tween-20, 0.05% sodium azide in 10 mMPBS.
[0031] 2) Using 10mM, pH 7.4 PBS, adjust the concentration of cTnI-coated antibody, Myo-coated antibody and goat anti-mouse IgG antibody to 1mg / ml, respectively, and print the three on the nitrocellulose membrane evenly, and then in 37 ℃ drying oven for 12 hours, add desiccant and seal for later use.
[0032] 3) Using a nano-gold solution with a diameter of 13nm, using 0.2M K 2 CO 3 Adjust the pH of the solution to 8.5, add cTnI capture antibody to adjust the final concentration to 8 μg / ml, let it stand at room temperature for 30 minutes, then add biotinylated single-stranded DNA to make the final concentration 1 μM, and let it stand at room temperature for 16 hours. Then add a final con...
Embodiment 2
[0055] 1) After soaking the sample pad in the sample pad treatment solution for 60 minutes, take it out and dry it in a drying oven at 45°C for 18 hours, then add a desiccant and store it for later use; the sample pad treatment solution contains 1% BSA, 0.05% Tween- 20, 0.05% sodium azide in 10 mM PBS.
[0056] 2) Using 10mM, pH 7.4 PBS, adjust the concentration of cTnI-coated antibody, Myo-coated antibody and goat anti-mouse IgG antibody to 1mg / ml, respectively, and print the three evenly on the nitrocellulose membrane, and then in 45 ℃ drying oven for 18 hours, adding a desiccant and storing for later use.
[0057] 3) Using a nano-gold solution with a diameter of 13nm, using 0.2M K 2 CO 3 Adjust the pH value of the solution to 8.5, add cTnI capture antibody to adjust the final concentration to 8 μg / ml, let it stand at room temperature for 30 minutes, then add biotinylated single-stranded DNA to make the final concentration 1 μM, and let it stand at room temperature for 16 ...
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