A method for detecting metal ions based on hybridization chain reaction signal amplification technology
A technology of hybridization chain reaction and technical detection, which is applied in the direction of biochemical equipment and methods, measurement/inspection of microorganisms, electrochemical variables of materials, etc., can solve problems such as threats to aquatic organisms and human health, and achieve high selectivity and resistance Interference ability, enhanced selectivity, wide linear range effect
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Embodiment 1
[0033] Example 1 A combined detection of heavy metal Ag based on magnetic nanoparticles and hybridization chain reaction amplification technology+ ionic method
[0034] The invention is based on the combined use of magnetic nanoparticles and hybrid chain reaction amplification technology to detect heavy metal Ag + The principle of the ionic method is as follows figure 1 shown. C-base-rich nucleic acid strand S1 is fixed to Fe via Au-S bond 3 o 4 @Au core-shell magnetic nanoparticle surface, on the target silver ion Ag + In the presence of ferrocene-labeled another C base-rich nucleic acid strand S2 passes through the C-Ag + The -C structure forms double-stranded DNA with S1 on the surface of the magnetic particle. When ferrocene-labeled hairpin DNA H1 and H2 are added, the hairpin-shaped H1 and H2 are opened under the induction of S2 and hybridization chain reaction occurs on the surface of magnetic nanoparticles, and the formed long-chain DNA complex passes through The ...
Embodiment 2
[0035] Embodiment 2 Oligonucleotide sequence design
[0036] The oligonucleotide sequence designed in the present invention was synthesized by China Shanghai Sangon Bioengineering Co., Ltd., purified and tested by HPLC, and freeze-dried. The oligonucleotide sequence designed by the present invention is as follows:
[0037] S1: 5'-SH-CAC TTC TCT CTT CTC TTC CCT CTC-3';
[0038] S2: 5’-AGG AGT AGA CTA GAT CGG ACA CAC ACC CAA CAC AAC ACA CAA CTC-NH 2 -3';
[0039] H1: 5’-TGT CCG ATC TAG TCT ACT CCT ACT GTG AGG AGT AGA CAT GAT-NH 2 -3';
[0040] H2: 5’-AGG AGT AGA CTA GAT CGG ACA ATC TAG TCT ACT CCT CAC AGT-NH 2 -3';
[0041] The oligonucleotides were dissolved in ultrapure sterile water and stored at -18°C for later use.
Embodiment 3
[0042] Example 3 Fe 3 o 4 Preparation of @Au core-shell magnetic nanoparticles
[0043] Take 1 g FeCl 2 4H 2 O, 2.6 g FeCl 3 6H 2 O and 0.425 mL of concentrated HCl were dissolved in 100 mL of water, and ultrasonically deoxygenated. Add the above mixture dropwise to 125 mL 0.75 M NaOH solution, N 2 Stir at 80°C under protection to get Fe 3 o 4 magnetic nanoparticles. Prepare 5 g / L of Fe 3 o 4 Ethanol solution 25 mL, ultrasonically dispersed, dropwise added 0.4 mL 3-aminopropyltriethoxysilane, stirred at room temperature for 7 h, diluted to 1 g / L, added 14 mL 0.6 M HAuCl 4 3H 2 O and 0.3 mL of 0.2 M sodium citrate solution, sonicated at room temperature, the color of the solution changed from light yellow to black, and Fe 3 o 4 @Au core-shell magnetic nanoparticles, magnetic separation and washing, dry storage.
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