Activated fluorescent latex microspheres for ferritin fluorescent immunochromatographic detection card
A technology of fluorescent latex microspheres and fluorescent immunochromatography, applied in analytical materials, luminescent materials, biological testing, etc., can solve problems such as reduced detection sensitivity, uneven dispersion, and chromatographic failure, and achieve stable and accurate detection results. Accurate, easy-to-operate results
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Embodiment 1
[0046] 1) Take the surfactant (2mg sodium laurylalanine, 3mg polyethylene glycol monolaurate and 5mg sodium stearate) first dissolved in 0.5M carbonic acid buffer solution of pH9.6 (H value to 9.6 ), then add in 0.1ml of DMF, 0.1ml of DMF, add 1mg of N,N'-dicyclohexylcarbodiimide (DCC) and 0.6mg of N-hydroxysuccinimide (NHS) and stir at room temperature 3 hours.
[0047] 2) Adjust the pH value of 1ml of fluorescent latex microsphere solution containing 1% solids on the amino surface to 9.6 with 0.5M carbonic acid buffer solution of pH 9.6, then add it to step 1), and continue to stir and react for 3 hours. Acquired activated latex microspheres.
[0048] 3) Use a high-speed centrifuge to centrifuge the fluorescent latex microsphere reaction solution at high speed, remove the supernatant of the reaction solution, and redissolve the fluorescent latex microspheres with 1mL microsphere buffer to form a marker working solution.
[0049] Microsphere phosphate buffer preparation: 0....
Embodiment 2
[0051] The operation method of this example is similar to that of Example 1, except that the surfactant in step 1) is: 0.5mg sodium laurylalanine, 2.5mg polyethylene glycol monolaurate and 5mg hard sodium fatty acid.
Embodiment 3
[0053] The operation method of this example is similar to that of Example 1, except that the surfactant in step 1) is: 5 mg sodium laurylalanine, 0.5 mg polyethylene glycol monolaurate and 4.5 mg hard sodium fatty acid.
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