Precise pathogenic microorganism detection and killing method of intelligent bioprobe
A technology of pathogenic microorganisms and biological probes, applied in the biological field, can solve problems such as harshness, narrow acid-base range, complex programming, etc., and achieve the effect of instant detection, high sensitivity, and good universality
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Embodiment 1
[0027] A real-time, rapid and accurate detection method for pathogenic microorganisms based on intelligent biological probes such as in situ self-assembly programmable nucleic acid, the specific steps are as follows:
[0028] The chloroauric acid solution prepared with sterile water was used as the gold ion precursor solution in this embodiment, mixed with Escherichia coli, and then continued to add a certain concentration of DNA solution diluted with sterile water as the experimental group. Wherein the final concentration of the chloroauric acid solution is 200 μmol / L, and the final concentration of the DNA solution is 20 nmol / L. At the same time, a normal control group and a blank group were set up. Mix the above mixture thoroughly and place it on a constant temperature shaker to continue incubating for 0.5h, 1h, or 2-12h. Then take a small amount of the above-mentioned mixture and add it onto the glass slide, and seal the slide with a cover glass. Excited under a laser co...
Embodiment 2
[0031] A real-time, rapid and accurate detection method for pathogenic microorganisms based on intelligent biological probes such as in situ self-assembly programmable nucleic acid, the specific steps are as follows:
[0032] The silver nitrate solution prepared with sterile water was used as the silver ion precursor solution in this embodiment, which was mixed with Escherichia coli, and then a certain concentration of DNA solution diluted with sterile water was added as the experimental group. The final concentration of the silver nitrate solution is 200 μmol / L, and the final concentration of the DNA solution is 20 nmol / L. At the same time, a normal control group and a blank group were set up. Mix the above mixture thoroughly and place it on a constant temperature shaker to continue incubating for 0.5h, 1h, or 2-12h. Then take a small amount of the above-mentioned mixture and add it onto the glass slide, and seal the slide with a cover glass. Excited under a laser confocal ...
Embodiment 3
[0035] A real-time, rapid and accurate detection method for pathogenic microorganisms based on intelligent biological probes such as in situ self-assembly programmable nucleic acid, the specific steps are as follows:
[0036] Chlorauric acid solution and silver nitrate solution configured with sterile water are used as the gold and silver ion precursor solution of this embodiment, mixed with Escherichia coli, and then continue to add a certain concentration of DNA solution diluted with sterile water as an experiment Group. Wherein the final concentration of the chloroauric acid solution and the silver nitrate solution is 200 μmol / L, and the final concentration of the DNA solution is 20 nmol / L. At the same time, a normal control group and a blank group were set up. Mix the above mixture thoroughly and place it on a constant temperature shaker to continue incubating for 0.5h, 1h, or 2-12h. Then take a small amount of the above-mentioned mixture and add it onto the glass slide,...
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