A colorimetric method for detecting thrombin
A thrombin and colorimetric technology, applied in the field of biochemical analysis, can solve problems such as waste of resources and cumbersomeness, and achieve the effects of improving detection sensitivity, ultra-high-sensitivity detection, and increasing the amount of DNase
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Embodiment 1
[0033] Experimental part of embodiment 1
[0034] 1. Modification of 96-well plate:
[0035] (1) Add 200 μL of 5 mM glutaraldehyde to 6 microwells of a 96-well plate, shake in a water bath at 37° C. in a wet box for 4 hours, and coat the bottom of the microwells with glutaraldehyde.
[0036] (2) The reaction solution was discarded, the 6 microwells were washed 5 times with PBS of pH 5 and water respectively, and 200 μL of 1×10 -6 The capture probe of M (5'-GACGGCGAAGGATTGATACT-3') was placed in a water bath at 37°C for 4 hours, and the capture probe was modified onto the microwell plate.
[0037] (3) Discard the reaction solution, wash 6 microwells once with 200 μL water, add 25 μL 1×10 -6 M circular template (5′-CTTCGCCGTCCCCAACCCGCCCTACCCGGTTGGTGTGGTTGGCCCAACCCGCCTACCCAGTATCAATC-3′), 3 μL of 10×T4 ligase buffer, after 90°C for 10 min, annealed at room temperature for 1 h, and the circular template was connected to the capture probe on the surface of the microwell plate.
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