Method for detecting platelet antibody specificity by using flow cytometry and detection kit
A platelet antigen specific technology, applied in the direction of measuring devices, instruments, scientific instruments, etc., can solve the problem of scarcity of detection methods and achieve the effect of less sample consumption, simple steps and accurate results
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Embodiment 1
[0029] Example 1: Platelet Antibody Specific Detection Kit
[0030] A detection kit for detecting the specificity of platelet antibodies by flow cytometry, comprising platelet antigen-specific fluorescent microspheres coated with different anti-platelet-specific glycoprotein antibodies on the surface of different fluorescent microspheres, and microsphere buffer solution, platelet standards, platelet lysate, calibration beads, and detection antibodies.
Embodiment 2
[0031] Example 2: Preparation of a specific detection kit for platelet antibody detection by flow cytometry.
[0032] This embodiment is the preparation of the platelet antibody specific detection kit, which is carried out according to the following steps:
[0033] 1. Preparation of microsphere buffer
[0034] The microsphere buffer solution involved in this example is a PBS solution containing 5% FBS by volume. NaN3 (w / v), mix well, and filter through 0.45 μm water filter membrane.
[0035] 2. Preparation of platelet antigen-specific fluorescent microspheres
specific Embodiment approach
[0036]All platelet antigen-specific fluorescent microspheres of the present invention are prepared by coating anti-platelet-specific glycoprotein antibodies on carboxylated polystyrene microspheres labeled with APC fluorescein. The method is the same as the reaction system, so this embodiment Take the preparation of anti-CD109 antibody-specific fluorescent microspheres as an example. The specific implementation is as follows:
[0037] 2.1 Solution preparation
[0038] 2.1.1 Preparation of buffer A: Weigh 0.96g NaH2PO4•2H2O, add H2O 600mL to dissolve, adjust the pH value to 6.0, add H2O to the volume to 800 mL, filter with 0.45 μm water filter membrane;
[0039] 2.1.2 Preparation of buffer B: Weigh 7.5g of glycine, add 800mL of H2O to dissolve, adjust the pH value to 7.5, add H2O to the volume to 1000mL, and filter with a 0.45 μm water filter membrane;
[0040] 2.1.3 Preparation of 50 mg / mL 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC) solution: Weigh 1 g ...
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