Lead ion detection test paper and preparation method thereof
A technology for detecting test strips and lead ions, which is applied in biochemical equipment and methods, microbiological determination/inspection, etc., can solve the problems of low sensitivity, high analysis cost, poor selectivity, etc., and achieve the effect of high sensitivity
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Embodiment 1
[0042] The present invention is a lead ion detection test strip, the test strip consists of a strip base plate 1 and a sample pad 2 sequentially overlapped on the strip base plate 1, coated with a specific barcode DNA-nano gold-deoxyribozyme probe Composed of glass fiber binding pad 3, specific coated nitrocellulose membrane 4, and water-absorbing pad 5, the specific barcode DNA-nanogold-DNAzyme probe is bound to biotin at one end of the DNAzyme, and its other end is bound to There are nano-gold, and several barcode DNAs are combined on the surface of the nano-gold. The linear quality control line C line 6 is coated with streptavidin on the nitrocellulose membrane and bound with biotinylated capture DNA and streptavidin. The complex is coated with a linear detection line T line 7, and the base of the captured DNA is complementary to the base of the barcode DNA on the surface of the specific barcode DNA-nanogold-deoxyribozyme probe,
[0043] The structure of the specific barcod...
Embodiment 2
[0051] A kind of preparation method of lead ion detection test strip of the present invention, concrete steps are as follows:
[0052] 1. Preparation of sample pad 2
[0053] Soak the glass fiber paper with 0.01-0.05 mol / L Tris-HCl buffer solution to wet it, and then dry it at 20°C-37°C for 4-12 hours to obtain a sample pad. The mass fraction of sucrose contained in the Tris-HCl buffer solution is 1~10%, pH value is 5.0~8.0.
[0054] 2. Preparation of glass fiber binding pad 3 coated with specific barcode DNA-nanogold-deoxyribozyme probe
[0055] Soak the glass fiber paper with 0.01-0.05 mol / L Tris-HCl buffer solution (the mass fraction of Tris-HCl buffer solution containing sucrose is 1-10%, and the pH value is 5.0-8.0). After drying at 37°C for 4 to 12 hours, evenly spray 2.0 to 10.0 μL of specific barcode DNA-nanogold-deoxyribozyme probe solution on each square centimeter of glass fiber paper, and dry at 20°C to 37°C for 2 After ~5 hours, the glass fiber binding pad 3 co...
Embodiment 3
[0065] The present invention is a lead ion detection test strip, the test strip consists of a strip base plate 1 and a sample pad 2 sequentially overlapped on the strip base plate 1, coated with a specific barcode DNA-nano gold-deoxyribozyme probe Composed of glass fiber binding pad 3, specific coated nitrocellulose membrane 4, and water-absorbing pad 5, the specific barcode DNA-nanogold-DNAzyme probe is bound to biotin at one end of the DNAzyme, and its other end is bound to There are nano-gold, barcode DNA is combined on the surface of nano-gold, and streptavidin is used to coat the linear quality control line C line 6 on the nitrocellulose membrane, and the complex of biotinylated capture DNA and streptavidin is used. Object-coated linear detection line T line 7, the base of the captured DNA is complementary to the base of the barcode DNA on the surface of the specific barcode DNA-nanogold-deoxyribozyme probe, and its specific preparation is as follows:
[0066] 1. Preparat...
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