Chemiluminescence immune analytic reagent kit for detecting tuberculosis antibody
A technology of chemiluminescent immunity and tuberculosis antibody, which is applied in the field of immunoanalysis medicine to achieve the effect of ensuring sensitivity and specificity
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Embodiment 1
[0021] Example 1 Preparation of tuberculosis antibody chemiluminescence immunoassay detection kit of the present invention
[0022] The tuberculosis antibody assay kit of the present invention comprises: streptavidin-coated microwell plate, negative and positive controls, biotinylated tuberculosis antigen, alkaline phosphatase-labeled tuberculosis antigen, concentrated washing solution and chemiluminescence substrate solution;
[0023] 1. Preparation of streptavidin-coated microwell plates
[0024] (1) Coated
[0025] Mix 0.05M PBS buffer solution with a pH value of 7.2 and appropriate concentration of streptavidin to make a coating solution, add it to the luminescence plate, 100 μL per well, and overnight at 4 °C;
[0026] Specifically, the PBS buffer preparation method is 2.2gNaH 2 PO 4 2H 2 O, 12.9gNa 2 HPO 4 12H 2 O, 9gNaCl, dilute to 1000mL with purified water, adjust pH to 7.2.
[0027] (2) closed
[0028] Prepare casein blocking solution, respectively add 12.1...
Embodiment 2~3
[0047] Embodiment 2~3 preparation tuberculosis antibody chemiluminescence immunoassay detection kit of the present invention
[0048] Except for using plastic beads and plastic tubes as carriers, the tuberculosis antibody chemiluminescence immunoassay detection kit was prepared in the same manner as in Example 1.
Embodiment 4
[0049] Embodiment 4 The using method of kit of the present invention
[0050] 1) Take out the kit from the refrigerator at 4°C, and equilibrate at room temperature for 30 minutes;
[0051] 2) Dilute the concentrated washing solution provided by the kit 25 times with purified water before use;
[0052] 3) Add 50 μL of biotinylated antigen to each well; then set 3 wells for negative control, 50 μL for each well; 2 wells for positive control, 50 μL for each well; 1 well for blank, add 50 μL of sample to be tested in the remaining wells, and use a micro shaker Shake and mix well, affix the sealing film, and incubate at 37°C for 30 minutes;
[0053] 4) Wash the plate 5 times, 400 μL per well, and finally dry it on clean absorbent paper;
[0054] 5) Add 50 μL of enzyme markers to the remaining wells except for the blank well, vortex and mix well, stick the sealing film on the plate, and incubate at 37°C for 30 minutes;
[0055] 6) Wash the plate 3 times, 400 μL per well, and fina...
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