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. 2014 Jul 4;4:5578. doi: 10.1038/srep05578

Figure 1. Fluorescent probes to detect the NER dual incisions.

Figure 1

(a) A linear duplex containing the (6–4) photoproduct and the fluorophore–quencher pair. Detection of the dual incisions in cells was not successful due to nonspecific degradation. (b) A plasmid-type probe containing the fluorophore and the quencher in the same strand. Degradation of the dual-incision product by cellular nucleases was expected to obtain the positive signal.