Procalcitonin detection test strip and preparation method thereof
A procalcitonin and detection test paper technology, which is applied in the biological field to achieve the effect of rapid detection means and sensitivity improvement
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Embodiment 1
[0040] Example 1: Preparation of conjugate release region
[0041] Add 2 μmol of quantum dots with a particle size of 5 nm, an excitation wavelength of 365 nm, and an emission wavelength of 605 nm and 1 mg of anti-human procalcitonin monoclonal antibody (purchased from Shenzhen Berrault Biological Products) into 1 mL of pH7.4 and 50 mM phosphate buffer solution. Co., Ltd.), shake gently at room temperature for 2 hours, then centrifuge at 12,000 r / min for 30 minutes, and take the precipitate to obtain the quantum dot-labeled procalcitonin monoclonal antibody.
[0042] After the quantum dot-labeled procalcitonin monoclonal antibody is treated with a stabilizer, it is evenly sprayed on the glass cellulose membrane at an amount of 65 μL per square centimeter, and freeze-dried to obtain the conjugate release area.
Embodiment 2
[0043] Embodiment 2: the preparation of reaction area
[0044] Spray 10 μL of 1 mg / mL procalcitonin on the nitrocellulose membrane in the reaction area, and freeze-dry to obtain the test area.
[0045] Spray 10 μL of 1 mg / mL anti-mouse IgG antibody (purchased from Shenzhen Berrault Biological Products Co., Ltd.) on the nitrocellulose membrane in the reaction area, and freeze-dry to obtain the control area.
Embodiment 3
[0046] Embodiment 3: the preparation of test strip
[0047] The sample application area, the conjugate release area obtained in Example 1, the reaction area obtained in Example 2, and the water absorption area are successively pasted on the backing to overlap each other.
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