Impedance type aptamer sensor for detecting lead ions based on gold nanomaterial and dendritic DNA nanostructure
An aptamer sensor and nanostructure technology, which is applied to the analysis of materials, electrochemical variables of materials, and material analysis through electromagnetic means, can solve the problems of high detection costs, expensive instruments, and high technical requirements for operators, and achieve repeatability. Good performance, fast response and high sensitivity
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Embodiment 1
Specific steps are as follows:
(1) Formation of Y-DNA structure: Accurately pipette 2.5 μL of each of the three ssDNA (m, n, q) of 1 μmol / L into a 200 μL centrifuge tube, vortex to mix well, and set the PCR machine to 95 °C for 5 min, then slowly cooled to 4 °C and held for 30 min to complete the annealing procedure to form a Y-DNA structure.
[0016] (2) The construction of impedance-type aptamer sensor includes two parts: Y-DNA structure system and electrode system. Electrode system: Incubate 5 μL of gold nanoflower material on the electrode surface for 2 h, and then bind 5 μL of complementary strand, 2 μmol / L cDNA to the electrode surface in the form of Au-S for 2 h. When the sample contains lead ions, the aptamer chain Apt binds to the lead ions, so that the anchorDNA, the H1-H2 mixed solution of the hairpin and the Y-DNA structure are combined with the complementary strand cDNA on the electrode at a concentration ratio of 1 / 1 / 1. Finally, Rinse the electrode with phospha...
Embodiment 2
Specific steps are as follows:
(1) Formation of Y-DNA structure: Accurately pipette 2.5 μL of each of the three ssDNA (m, n, q) at 2 μmol / L into a 200 μL centrifuge tube, vortex to mix well, and set the PCR machine to 100 °C for 10 min, and then slowly cooled to 10 °C for 45 min to complete the annealing procedure to form a Y-DNA structure.
[0019] (2) The construction of impedance-type aptamer sensor includes two parts: Y-DNA structure system and electrode system. Electrode system: 7 μL of gold nanorod material was incubated on the electrode surface for 1.5 h, and then 7 μL of complementary strand, 4 μmol / L cDNA was bound to the electrode surface in the form of Au-S for 1.5 h. When the sample contains lead ions, the aptamer chain Apt binds to the lead ions, so that the anchor DNA, the hairpin H1-H2 mixed solution and the Y-DNA structure are combined with the complementary strand cDNA on the electrode at a concentration ratio of 1 / 2 / 2. Finally rinse the electrode with phtha...
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