Telomerase inhibitor screening system based on SPR technology
A technology of telomerase inhibitor and telomerase, which is applied in the direction of measuring devices, material analysis through optical means, instruments, etc., can solve the problems of high cost, long time, heavy workload, etc., and achieve the goal of speeding up the screening and development work Effect
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example 1
[0037] 1) the preparation of kit, it has first reaction solution, second reaction solution and diluent, described first reaction solution comprises the phosphate buffer of 10mmol / L and the dNTP of 100mmol / L, the pH of described buffer is 7.3; the second reaction solution comprises 100000U / ml of telomerase and a pH of 7.3 telomerase stock solution, and the telomerase stock solution comprises 10mmol / L PB buffer, 3mmol / L MgCl 2And 8wt% glycerol, the pH of the stable solution is 7.3; the diluent is a 10mmol / L PB buffer solution with a pH of 7.3, which is used to separate the first reaction solution and the second reaction solution in the actual test process. Dilute to appropriate concentration of dNTP and telomerase test working solution;
[0038] 2) Construction of the chip: After coating a silver film with a thickness of 43 nm on the glass slide, place it in a 5 μmol / L solution of thiol-modified telomeric DNA and incubate at 0°C for 10 hours, and connect the telomere DNA to the ...
example 2
[0041] 1) the preparation of kit, it has first reaction solution, second reaction solution and diluent, described first reaction solution comprises the phosphate buffer of 200mmol / L and the dNTP of 120mmol / L, the pH of described buffer It is 7.3; the second reaction liquid comprises telomerase of 100000U / ml and pH is the telomerase stock solution of 7.3, and the telomerase stock solution comprises the MgCl of 200mmol / L PBS damping fluid, 15mmol / L 2 And 10wt% glycerol, the pH of the stable solution is 7.3; the diluent is a 200mmol / L PBS buffer solution with a pH of 7.3, which is used to separate the first reaction solution and the second reaction solution in the actual test process. Dilute to appropriate concentration of dNTP and telomerase test working solution;
[0042] 2) Construction of the chip: After plating a layer of gold film with a thickness of 46 nm on the glass slide, place it in 15 μmol / L telomeric DNA solution modified with trithioadamantane derivatives and incuba...
example 3
[0048] 1) the preparation of kit, it has first reaction solution, second reaction solution and diluent, described first reaction solution comprises the phosphate buffer of 100mmol / L and the dNTP of 110mmol / L, the pH of described buffer 7.3; the second reaction solution comprises 100000U / ml of telomerase and a pH of 7.3 telomerase stock solution, and the telomerase stock solution comprises 100mmol / L PB buffer, 10mmol / L MgCl 2 And 9wt% glycerol, the pH of the stable solution is 7.3; the diluent is a 100mmol / L PBS buffer solution with a pH of 7.3, which is used to separate the first reaction solution and the second reaction solution in the actual test process. Dilute to appropriate concentration of dNTP and telomerase test working solution;
[0049] 2) Construction of the chip: After plating a layer of gold film with a thickness of 44nm on the glass slide, place it in a 10 μmol / L solution of thiol-modified telomeric DNA and incubate at 5°C for 18 hours, and connect the telomeric ...
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