Detection method for rapidly and definitely diagnosing feline leukemia and preparation of test strip thereof
A technology for preparing test strips and antibodies, which is applied in the field of medical testing, can solve problems such as poor accuracy, low sensitivity, and weak detection signals of colloidal gold, and achieve the effect of saving detection time
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Embodiment 1
[0036] A fluorescent stability verification of a fluorescent microsphere-labeled antibody for feline leukemia detection, comprising the following steps:
[0037] (1) Add a quantitative fluorescent latex microsphere solution to a buffer solution for dilution, and ultrasonicate for 1.5 min to obtain a fluorescent microsphere dispersion.
[0038] (2) Quickly drop the activator into the fluorescent latex microsphere dispersion in step (1), place it on a vortex shaker for 1 minute at a low speed, fix it on a vortex shaker, and shake it at room temperature for 30 minutes to activate.
[0039] (3) After the activation, the fluorescent latex microsphere dispersion in step (2) was centrifuged at 26° C. at 14000 rpm for 12 minutes, then the supernatant was removed, washed with the buffer solution in step (1), and then washed with the same method again. After conditioned centrifugation, discard the supernatant and reconstitute and resuspend with the buffer solution in step (4).
[0040]...
Embodiment 2
[0059] A preparation method for a test strip for rapid detection of feline leukemia virus, comprising the following steps:
[0060] (1) Add a quantitative fluorescent latex microsphere solution to a buffer solution for dilution, and ultrasonicate for 1.5 min to obtain a fluorescent microsphere dispersion.
[0061] (2) Quickly drop the activator into the fluorescent latex microsphere dispersion in step (1), place it on a vortex shaker for 1 minute at a low speed, fix it on a vortex shaker, and shake it at room temperature for 30 minutes to activate.
[0062] (3) After the activation, the fluorescent latex microsphere dispersion in step (2) was centrifuged at 26° C. at 14000 rpm for 12 minutes, then the supernatant was removed, washed with the buffer solution in step (1), and then washed with the same method again. After conditioned centrifugation, discard the supernatant and reconstitute and resuspend with the buffer solution in step (4).
[0063] (4) FeLv monoclonal antibody ...
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