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. 2017 Sep 26;7:12335. doi: 10.1038/s41598-017-12549-3

Figure 4.

Figure 4

High throughput printing of DNAzyme and evaluation of signal levels upon addition of target sample. The DNAzyme probe was printed onto two paper devices using a Biodot printer, followed by drying. Fluorescence signaling was evaluated by adding the reaction buffer (A) and E. coli cell lysate (B) using the Biodot printer to ensure consistent sample volumes were dispensed. After the cleavage reaction, the fluorescent signal was quantified and plotted (C). The standard deviation (SD) was calculated from 84 individual experiments on paper.