Fluorescence immunoassay method of using zinc oxide quantum dots to mark antibody
A determination method and fluorescence immunological technology, applied in fluorescence/phosphorescence, biological testing, measurement devices, etc., can solve the problems of delayed disease discovery and optimal treatment timing, long cycle, poor accuracy, etc., to achieve rapid and convenient testing, conditions Controlled, mildly conditioned effects
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[0027] (Such as figure 2 )
[0028] Step 1: Add 0.55 g of zinc acetate dihydrate to 25 ml of ethanol, reflux at 80°C for 3 hours, dissolve the zinc acetate, and cool to room temperature.
[0029] Step 2: Add 0.148 g of lithium hydroxide monohydrate to 25 ml of ethanol, and ultrasonically dissolve it for 10 minutes.
[0030] The third step: mix the solution obtained in the first step and the second step, add ethanol to dilute it 10 times, place it in an autoclave, and seal it so that it can withstand a pressure of not less than 2×10 5 Pa, heated to 70° C., kept for 1 hour, naturally cooled to room temperature, taken out, centrifuged, and washed three times with deionized water to obtain zinc oxide quantum dots.
[0031] Step 4: Disperse 5 mg of zinc oxide quantum dots into 100 μl of 5 μg / ml CA19-9 antibody solution, shake at 35° C. for 1 hour, centrifuge, and wash three times with pH7.4 phosphate buffer solution. Finally, it is dispersed in 1 ml of pH7.4 phosphate buffer so...
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