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. 2016 Aug 26;16(9):1370. doi: 10.3390/s16091370

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© 2016 by the authors; licensee MDPI, Basel, Switzerland.

This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/).

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(A) The secondary structure of the Ag10c DNAzyme. For the Tb³⁺ luminescence experiment, the substrate is the all-DNA analog and cannot be cleaved; (B) Tb³⁺ luminescence spectroscopy with the Ag10c DNAzyme in the presence of 0, 0.1, 1 and 10 µM concentrations of Ag⁺; (C) A scheme showing the effect of Ag⁺ in promoting the luminescence of poly G, T DNA.