Kit and method for joint detection based on microspheres with different fluorescence intensities
A fluorescence intensity and combined detection technology, which is applied in fluorescence/phosphorescence, measuring devices, and material analysis through optical means, can solve problems such as inability to detect, and achieve full response, accurate results, and stable detection results.
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Embodiment 1
[0030] A combined detection kit based on microspheres with different fluorescence intensities, the kit includes microsphere reagents, labeled second antibodies or antigens; the microsphere reagents are N types of microspheres with the same diameter and different fluorescence intensities, The surface of the sphere corresponds to the first antibody or antigen coated with N blood markers, where N is an integer between 2 and 5; the labeled second antibody or antigen includes the second antibody or antigen of N blood markers, and the second The antibody or antigen is labeled with fluorescein, and the binding sites of the first antibody or antigen, the second antibody or antigen and the corresponding antigen or antibody are different.
[0031] When N is 5, the preparation method of this microsphere reagent comprises the steps:
[0032] Step 101: Select five microspheres with the same diameter and different fluorescence intensity codes, and coat five different specific antigens or an...
Embodiment 2
[0093] A joint detection method based on microspheres of different fluorescence intensities, the method utilizes the kit for joint detection based on microspheres of different fluorescence intensities in Example 1, specifically comprising the following steps, such as Figure 1-2 Shown:
[0094] S101: adding the sample to be tested into the kit and incubating with the microsphere reagent inside to form a first reactant; the sample to be tested is one of whole blood and serum.
[0095] It should be understood that the microsphere reagent is the microsphere reagent mentioned in Example 1.
[0096] S102: adding a labeled second antibody or antigen to the first reactant for incubation to obtain a second reactant;
[0097] It should be understood that the labeled secondary antibody or antigen is prepared in the manner mentioned in Example 1.
[0098] S103: Detect the fluorescent signals of the blood markers on the surface of the N immune microspheres in the second reactant, so as ...
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