Method for labeling antibodies by colorful fluorescent granules and test paper strip prepared from antibodies
A technology for antibody preparation and test strips, which is applied in the field of colored fluorescent particle-labeled antibodies and test strips prepared using them, can solve problems such as weak signals, inconspicuous color development of test lines, and large differences between batches of quantitative detection. The effect of high sensitivity
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Embodiment 1
[0035] A test strip prepared by the canine distemper virus antibody labeled with colored fluorescent microspheres, comprising the following steps:
[0036] (1) Add a quantitative amount of colored fluorescent latex microsphere solution to the buffer solution for dilution, and ultrasonicate for 1.5 min to obtain a colored fluorescent microsphere dispersion.
[0037] (2) Quickly drop the activator into the dispersion of colored fluorescent latex microspheres in step (1), quickly place it on a vortex shaker and vibrate at a low speed for 1 minute, fix it on a vortex shaker, and activate it by shaking at room temperature for 30 minutes .
[0038] (3) After the activation, centrifuge the dispersion of colored fluorescent latex microspheres in step (2) at 14,000 rpm for 12 minutes at 26°C, remove the supernatant, wash with the buffer solution in step (1), and wash again After centrifugation under the same conditions, discard the supernatant and reconstitute and resuspend with the b...
Embodiment 2
[0058] A test strip prepared by a colored fluorescent microsphere-labeled feline leukemia virus antibody, comprising the following steps:
[0059] (8) Add a quantitative amount of colored fluorescent latex microsphere solution to the buffer solution for dilution, and sonicate for 1.5 min to obtain a colored fluorescent microsphere dispersion.
[0060] (9) Quickly drop the activator into the dispersion of colored fluorescent latex microspheres in step (1), quickly place it on a vortex shaker and vibrate at a low speed for 1 minute, fix it on a vortex shaker, and activate it by shaking at room temperature for 30 minutes .
[0061] (10) After the activation, the colored fluorescent latex microsphere dispersion in step (2) was centrifuged at 14000rpm at 26°C for 12min to remove the supernatant, washed with the buffer solution in step (1), and washed again with After centrifugation under the same conditions, discard the supernatant and reconstitute and resuspend with the buffer so...
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