Kit for detecting ATP with nucleic acid aptamer and detection method thereof
A nucleic acid aptamer and kit technology, which is applied in measuring devices, instruments, scientific instruments, etc., can solve the problems of immune antibody preparation, stability, and cost limitations, and achieve poor stability, inactivation, and high accuracy Effect
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Embodiment 1
[0037] Example 1: Using nucleic acid aptamer AD25 or AD25-10P to detect ATP based on fluorescence anisotropy (fluorescence polarization)
[0038] The nucleic acid aptamer of this embodiment is a nucleic acid molecule with the sequence shown in SEQ ID NO.1 (abbreviated as AD25) or a nucleic acid molecule with the sequence shown in SEQ ID NO.2 (abbreviated as AD25-10P).
[0039] Incubate 10 nM TMR-labeled ATP, 5 μM nucleic acid aptamer AD25 (or AD25-10P) and different concentrations of ATP in the binding buffer solution, and then measure the fluorescence anisotropy value (r) or fluorescence polarization value (P) of TMR (Temperature is measured under 10 ℃), the result is as follows figure 2 with image 3 shown. The sequence of the nucleic acid aptamer AD25 is SEQ ID NO.1 (5'-CCT GGG GGA GTATTG CGG AGG AAG G-3'). The sequence of the nucleic acid aptamer AD25-10P is SEQ ID NO.2 (5'-ACT CAG CCGGCC TGG GGG AGT ATT GCG GAG GAA GGC CGG CTG AGT-3').
[0040] from figure 2 It can...
Embodiment 2
[0041] Example 2: Detection of ATP in diluted urine samples based on fluorescence anisotropy using aptamer AD25-10P
[0042] Incubate 10nM TMR-labeled ATP, 5μM AD25-10P, and different concentrations of ATP in urine samples diluted 20 times with binding buffer solution, and then measure the fluorescence anisotropy value (r) of TMR (measured at 10°C) , subtract the fluorescence anisotropy value corresponding to the blank sample to obtain the change value of the fluorescence anisotropy Δr. The results show that the ATP in the diluted urine sample can be detected, and the relationship between the change value Δr of the fluorescence anisotropy and the change of the ATP concentration can be found in Figure 4 .
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