Method for preparing carcinoembryonic antigen working electrode for screen printing electrode
A technology of screen printing electrodes and working electrodes is applied in the field of preparation of carcinoembryonic antigen working electrodes, and can solve the problems of reduced detection accuracy, difficulty in removal, sensitivity and service life effects, etc.
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Embodiment 1
[0020] A preparation method of a carcinoembryonic antigen working electrode of a screen printing electrode, comprising the steps of:
[0021] 1) Make the concentration 0.01~0.1mol·L -1 5-10 mL of Tris-HCl buffer solution was placed in a centrifuge tube, and then added with a concentration of 1 mg·mL -1 5-10 μL of GMP solution with a diameter of 10-50 nm and a concentration of 1-3 mg·mL -1 Horseradish peroxidase-labeled mouse anti-human CEA monoclonal antibody solution 10 μL, shaking reaction at 25-37°C for 20-30 minutes;
[0022] 2) Place the above-mentioned centrifuge tube in a magnetic separator, magnetically separate it under a magnetic field of 0.1-0.3mT for 3-10 minutes, and discard the supernatant, so that the CEA antibody is coated on the surface of GMP;
[0023] 3) Add pH 7.0 to the centrifuge tube with a concentration of 0.2-1mol·L -1 5 mL of PBS buffer and a concentration of 10-15 mg·mL -1 5 μL of BSA solution, stirred at room temperature for 1 hour, magnetically...
Embodiment 2
[0028] It is basically the same as Example 1, except that the horseradish peroxidase-labeled mouse anti-human CEA monoclonal antibody is made of horseradish peroxidase-labeled goat anti-human CEA monoclonal antibody or horseradish peroxidase-labeled goat anti- Mouse CEA monoclonal antibody surrogate.
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