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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[0041] Example 1
[0042] The present invention is a lead ion detection test strip. The test strip consists of a strip-shaped bottom plate 1 and a sample pad 2 which is sequentially overlapped on the strip-shaped bottom plate 1 and coated with a specific barcode DNA-nano-gold-deoxyribozyme probe The specific barcoded DNA-nano-gold-deoxyribozyme probe is composed of a glass fiber binding pad 3, a specially coated nitrocellulose membrane 4, and a water-absorbing pad 5. Biotin is bound to one end of the deoxyribozyme, and the other end is bound to There are nano-gold, several bar coded DNAs are bound on the surface of nano-gold, the linear quality control line C 6 is coated with streptavidin on the nitrocellulose membrane and combined with biotinylated capture DNA and streptavidin The complex is coated with the linear detection line T line 7, and the bases of the captured DNA are complementary paired with the bases of the barcoded DNA on the surface of the specific barcode DNA-nano-...
Example Embodiment
[0050] Example 2
[0051] The method for preparing a lead ion detection test strip of the present invention has the following specific steps:
[0052] 1. Preparation of sample pad 2
[0053] After soaking the glass fiber paper with 0.01~0.05 mol / L Tris-HCl buffer, it is dried at 20℃~37℃ for 4~12 hours to obtain the sample pad. The mass fraction of sucrose in Tris-HCl buffer is 1~10%, pH value is 5.0~8.0.
[0054] 2. Preparation of glass fiber binding pad 3 coated with specific barcode DNA-nano-gold-deoxyribozyme probe
[0055] The glass fiber paper is soaked and moistened with 0.01~0.05 mol / L Tris-HCl buffer (the Tris-HCl buffer contains 1-10% sucrose, and the pH value is 5.0-8.0), and then at 20℃~ After drying for 4-12 hours at 37℃, spray 2.0-10.0 μL of specific barcode DNA-nano-gold-deoxyribozyme probe solution evenly on every square centimeter of glass fiber paper and dry at 20℃~37℃2 After ~5 hours, the glass fiber binding pad 3 coated with specific barcoded DNA-nano-gold-deoxyri...
Example Embodiment
[0064] Example 3
[0065] The present invention is a lead ion detection test strip. The test strip consists of a strip-shaped bottom plate 1 and a sample pad 2 which is sequentially overlapped on the strip-shaped bottom plate 1 and coated with a specific barcode DNA-nano-gold-deoxyribozyme probe The specific barcoded DNA-nano-gold-deoxyribozyme probe is composed of a glass fiber binding pad 3, a specially coated nitrocellulose membrane 4, and a water-absorbing pad 5. Biotin is bound to one end of the deoxyribozyme, and the other end is bound to There is nano-gold, bar code DNA is bound to the surface of nano-gold, the linear quality control line C 6 is coated with streptavidin on the nitrocellulose membrane, and the combination of biotinylated capture DNA and streptavidin combined The substrate is coated with a linear detection line T line 7, and the bases of the captured DNA are complementary paired with the bases of the barcoded DNA on the surface of the specific barcode DNA-n...
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