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- W2773756985 abstract "The “Switching – On” complexes, indolium derivatives bound with nuclear acids, were used as fluorescence probes to recognize the endonuclease and monitor the enzyme activities. Three probes, H1, L1 and N1, weakly emitted in aqueous buffer, exhibited strong red emissions when they bound into DNA or RNA. For H1-RNA or L1-RNA, the fluorescence was sensitively quenched by endoribonuclease, RNase A. The quenching of H1 or L1 originated only from the cleavage of RNase A to RNA, which was proved by various control and interference experiments. The specific recognition and highly sensitive enzyme activity assay of RNase A was simply conducted based on H1-RNA or L1-RNA “Switching-ON” fluorescent complex, and the detection limit (DL) is as low as 2.87 × 10−7 U/mL for H1-RNA, and 5.02 × 10−7 U/mL for L1-RNA, respectively. This approach was also used to evaluate the efficiency of inhibitors for RNase A." @default.
- W2773756985 created "2017-12-22" @default.
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- W2773756985 date "2018-04-01" @default.
- W2773756985 modified "2023-10-01" @default.
- W2773756985 title "Highly sensitive and selective RNase A recognition systems based on “OFF – ON – OFF” fluorescence probes" @default.
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- W2773756985 doi "https://doi.org/10.1016/j.snb.2017.12.072" @default.
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