Magnetic bead-transformed Prussian blue avian influenza virus immune biosensor and method
A bird flu virus and biosensor technology, which is applied in the direction of instruments, scientific instruments, and electrochemical variables of materials, can solve time-consuming and cumbersome problems, and achieve the effects of broad application prospects, sensitive detection, and simple modification operations
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Embodiment 1
[0055] Put 15mL of magnetic bead aqueous solution in a 50mL centrifuge tube, and disperse for 5min under the action of ultrasound with a working frequency of 40kHz and a power of 160W to obtain a uniformly dispersed magnetic bead dispersion.
[0056] Then 15 mL of 0.4 M citric acid aqueous solution was added, ultrasonicated for 30 min, and rotated for 20 h at room temperature (25° C.). Perform magnetic separation, remove supernatant, and wash magnetic beads three times with phosphate buffer, then disperse in 15 mL of MES buffer (final concentration of magnetic beads is about 1 mg / mL), and store at 4°C.
[0057] Add EDC (2mg, 10mM) and NHS (0.35mg, 15mM) to 1mL of the above-mentioned functional magnetic bead dispersion, stir and react at room temperature for 2 hours, wash with phosphate buffer (pH 6.0) magnetically for three times, and then disperse in 1mL in phosphate buffer.
[0058] Take 100 μL of activated magnetic beads and 400 μL of concanavalin A (Con A) to react at roo...
Embodiment 2
[0067] Put 15mL of magnetic bead aqueous solution in a 50mL centrifuge tube, and disperse for 5min under the action of ultrasound with a working frequency of 40kHz and a power of 160W to obtain a uniformly dispersed magnetic bead dispersion.
[0068] Then add different volumes of 0.4M citric acid aqueous solution, so that the ratio of citric acid to magnetic bead dispersion is 0.1mmol, 0.2mmol and 0.3mmol per mg of magnetic nano material. Sonicate for 30 minutes, and rotate for 20 hours at room temperature (25° C.). Perform magnetic separation, remove supernatant, and wash magnetic beads three times with phosphate buffer, then disperse in 15 mL of MES buffer (final concentration of magnetic beads is about 1 mg / mL), and store at 4°C.
[0069] Add EDC (2mg, 10mM) and NHS (0.35mg, 15mM) to 1mL of the above-mentioned functional magnetic bead dispersion, stir and react at room temperature for 2 hours, wash with phosphate buffer (pH 6.0) magnetically for three times, and then disper...
Embodiment 3
[0074] Put 15mL of magnetic bead aqueous solution in a 50mL centrifuge tube, and disperse for 5min under the action of ultrasound with a working frequency of 40kHz and a power of 160W to obtain a uniformly dispersed magnetic bead dispersion.
[0075] Then 15 mL of 0.4 M citric acid aqueous solution was added, ultrasonicated for 30 min, and rotated for 20 h at room temperature (25° C.). Perform magnetic separation, remove supernatant, and wash magnetic beads three times with phosphate buffer, then disperse in 15 mL of MES buffer (final concentration of magnetic beads is about 1 mg / mL), and store at 4°C.
[0076] Add EDC (2mg, 10mM) and NHS (0.35mg, 15mM) to 1mL of the above-mentioned functional magnetic bead dispersion, stir and react at room temperature for 2 hours, wash with phosphate buffer (pH 6.0) magnetically for three times, and then disperse in 1mL in phosphate buffer.
[0077] Take 100 μL of activated magnetic beads and 400 μL of concanavalin A (Con A) to react at roo...
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