Biosensor as well as preparation method and application
A biosensor and reaction technology, applied in the field of biosensing, can solve the problems of small difference in color, photobleaching signal-to-noise ratio of biosensors, etc.
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Embodiment 1
[0047] Prepare the gold-silver core-shell-tetrahedral structure DNA assembly biosensor containing azobenzene molecules according to the following steps:
[0048] (1) Preparation of gold-silver core-shell nanoparticles
[0049] Take sodium borohydride reduction to prepare 3nm gold seeds, use the seed growth method to grow the 3nm gold seeds into 30nm gold balls, add 0.01M silver nitrate solution drop by drop, the measured ultraviolet spectrum is 505nm, and the gold and silver nuclei with a size of 50nm are obtained Shell nanoparticles (Au@AgNCs).
[0050] The specific process is as follows:
[0051] a. Preparation of about 3nm GNPs
[0052] Select a clean and treated 20mL glass bottle as the reaction bottle. Put the cleaned magnets into the reaction bottle, and ensure that the entire reaction device is in the middle of stirring. Then add 0.1M CTAB (aqueous, aqueous: aq) 10mL and 0.01M HAuCl to the reaction flask 4 (aq) 0.25mL, during the process of sample addition, stir wi...
Embodiment 2
[0071] The preparation method of present embodiment is identical with embodiment 1, and difference is:
[0072] In step (3), the tetrahedral DNA was diluted at a ratio of 1:100000, and 200 μL of tetrahedral DNA with a concentration of 10 pM was dropped onto the gold-silver core-shell nanoparticles immobilized on the surface of ITO.
Embodiment 3
[0074] The preparation method of present embodiment is identical with embodiment 1, and difference is:
[0075] In step (3), the tetrahedral DNA was diluted at a ratio of 1:10000, and 200 μL of tetrahedral DNA with a concentration of 100 pM was dropped onto the gold-silver core-shell nanoparticles immobilized on the surface of ITO.
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