Preparation method of electrochemiluminescence biosensor for detecting mercury ions
A luminescent biological and electrochemical technology, applied in the field of biosensors, can solve the problems of large-scale equipment and high operation requirements, and achieve the effect of simple preparation method, simplified complexity, and sensitive analysis and detection
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Embodiment 1
[0036] Concrete preparation method of the present invention is as follows:
[0037] (1)Ru(dcbpy) 3 2+ - Preparation of DNA1 composites:
[0038]Dissolve 4 mg of tris(4,4-dicarboxybipyridyl) ruthenium chloride in 8 mL of buffer solution (pH=7), add 2 mL of a mixed solution containing 160 mg of EDC and 40 mg of NHS into the above solution and stir at room temperature for 2 h, then add 1.6 mL of 0.5 -3μM DNA1 continued to stir for 6-12h, this time the stirring environment was 25°C, 100rpm, then added 800μL 0.5-5M sodium acetate solution and 16mL ethanol to carry out precipitation reaction at -30-1°C for 5-12h, and centrifuged at 12000rpm for 30min to obtain The precipitate was washed twice with 70% ethanol, and finally, after drying at room temperature, it was dissolved in 1 mL of buffer solution (pH=7) and placed in a refrigerator at 4°C for later use.
[0039] (2)g-C 3 N 4 Preparation of QDs-DNA2 composites:
[0040] 400μL mixture containing 40mM EDC and 10mM NHS added to...
Embodiment 2
[0050] Utilize the present invention to detect the liquid to be tested, the steps are as follows:
[0051] (1)Ru(dcbpy) 3 2+ - Preparation of DNA1 composites:
[0052] Dissolve 4 mg of tris(4,4-dicarboxybipyridyl) ruthenium chloride in 8 mL of buffer solution (pH=7), add 2 mL of a mixed solution containing 160 mg of EDC and 40 mg of NHS into the above solution and stir at room temperature for 2 h, then add 1.6 mL of 0.5 -3μM DNA1 continued to stir for 6-12h, this time the stirring environment was 25°C, 100rpm, then added 800μL 0.5-5M sodium acetate solution and 16mL ethanol to carry out precipitation reaction at -30-1°C for 5-12h, and centrifuged at 12000rpm for 30min to obtain The precipitate was washed twice with 70% ethanol, and finally, after drying at room temperature, it was dissolved in 1 mL of buffer solution (pH=7) and placed in a refrigerator at 4°C for later use.
[0053] (2)g-C 3 N 4 Preparation of QDs-DNA2 composites:
[0054] 400μL mixture containing 40mM E...
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