Activation fluorescence latex microsphere for gastrin 17 fluorescence immunochromatographic assay
A technology of fluorescent latex microspheres and fluorescent immunochromatography, which is applied in the analysis of materials, luminescent materials, and biomaterials. It can solve the problems of reduced detection sensitivity, uneven dispersion, and chromatographic failure, and achieve stable detection results. Accurate results and easy operation
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Embodiment 1
[0048] 1) Dissolve the surfactant (2mg polyethylene glycol monolaurate, 3.5mg sodium stearate, 0.5mg sodium lauryl dimethylene carbamate and 4mg sodium cocoyl glutamate) in 0.5M pH9.6 carbonic acid buffer (H value to 9.6), then add in 0.1ml of DMF, add N,N'-dicyclohexylcarbodiimide (DCC) 1mg and 0.6 mg N-hydroxysuccinimide (NHS) and stirred at room temperature for 3 hours.
[0049] 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.
[0050] 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.
[0051] Microsphere phosphate buffer prep...
Embodiment 2
[0053] The operation method of this example is similar to Example 1, except that the surfactant in step 1) is: 1 mg polyethylene glycol monolaurate, 5 mg sodium stearate, 1 mg dodecyl dimethylene Sodium Carbamate and 5mg Sodium Cocoyl Glutamate.
Embodiment 3
[0055] The operation method of this example is similar to that of Example 1, except that the surfactant in step 1) is: 2.5 mg polyethylene glycol monolaurate, 5 mg sodium stearate, 1.5 mg lauryl di Sodium methylene carbamate and 5 mg sodium cocoyl glutamate.
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