Preparation method of quantum dot electrochemical luminescence electrode based on deoxyribonucleic acid (DNA) charge transfer
A light-emitting electrode and charge transfer technology, applied in the field of electrochemiluminescence, can solve rare problems and achieve the effect of mild conditions and good electrochemiluminescence performance
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Embodiment 1
[0029] 1) Hybridization of double-stranded dsDNA: Melt the two single-stranded ssDNA stock solutions frozen in a shaker at room temperature. The sequences of the two single-stranded ssDNA are as follows: 5'-SH-GACTGACCTCGGACG and 5'-NH 2 -CGTCCGAGGTCAGTC. Mix the ssDNA stock solution with the same molar number respectively, place the mixed solution in a constant temperature water bath at 90°C for 5 minutes, and cool it to room temperature in a natural environment to form hybridized double-stranded dsDNA, and store it in a freezer at -20°C for later use;
[0030] 2) Preparation of 1mM 6-mercaptohexan-1-ol MCH: first prepare 5% glycerol phosphate buffer: use 5.0mM pH=7.0 phosphate buffer to make up the volume, after the volume is set up, vibrate evenly on the shaker, and save it for later use; Then prepare 1mM MCH: use the configured glycerol phosphate buffer solution to make up the volume, after the volume is set up, vibrate evenly on the oscillator, and save it for later use; ...
Embodiment 2
[0050] Step 1) 2) 3) 4) 5) 6) 7) 8) 9) 10) with embodiment 1;
[0051] 11) Rinse the electrode and place it in 0.1M pH=7.4 PB+0.1M K 2 S 2 o 8 In +0.1M KCl solution, the modified electrode was used as the working electrode, the platinum wire was used as the counter electrode, and the calomel electrode was used as the reference electrode for cyclic voltammetry scanning. The potential scanning range was 0.8 V ~ -1.8 V, and the scanning speed was is 100 mV / s.
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