Preparation method of spectral near-infrared electrochemical luminescence immunosensor
A chemiluminescence immunological and immunosensor technology, applied in the field of analysis, to achieve the effects of simple operation, rich content and detection index information, and high light intensity
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Embodiment 1
[0078] All the utensils were soaked in freshly prepared aqua regia for 24 hours, rinsed thoroughly with ultrapure water and ethanol, and then dried in the air; 0.4mM methionine, 0.25mL Au solution (96mM) and 1.2mL Ag solution ( 10mM) was dissolved in 4ml of ultrapure water and ultrasonically mixed, then 1M sodium hydroxide was added to adjust the pH value to 12.0, and incubated at 37°C for 10 hours. Centrifuge the prepared solution at 5000 rpm to remove large particles at the bottom, add 0.5 ml of 1M sulfuric acid solution to the supernatant, centrifuge and precipitate the initial gold nanoparticles at 8000 rpm, remove the supernatant, and add the final centrifuged precipitate to 3mL of 2% ammonia water, incubate in an oven at 80°C for 20 minutes, and finally centrifuge the prepared quantum dots with isopropanol at 13300 rpm, and store them in a refrigerator at 4°C. The fixed concentration of the bimetallic nanocluster solution is 1mg / mL Test the fluorescence spectrum, such as...
Embodiment 2
[0086] The steps are the same as in Example 1, except that the test method for the bimetallic nanocluster solution is an ultraviolet spectrogram, such as figure 2shown.
Embodiment 3
[0088] The steps are the same as in Example 1, except that the prepared bimetallic nanocluster solution is dropped on a copper grid to observe the morphology. The high-magnification transmission electron microscope photos of the gold-silver bimetallic nanoclusters made by the test, such as image 3 shown.
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