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. 2017 May 2;7:1347. doi: 10.1038/s41598-017-00758-9

Figure 3.

Figure 3

Multiplexed paper devices: performing several simultaneous reactions thanks to liquid flows. (a) Picture of an unfolded wax geometry (multilayered geometry), with dry amounts of dyes in the second last layer. Picture of the same device after folding and dipping it in water: the dyes are conveyed to the top without mixing together. (b) Schematics of the unfolded multilayered wax geometry and location of freeze-dried RT-RPA reagents and targeted RNA template. Exploded view of the folded device: the paper tape should be dipped into water and sample pipetted in the sample test outlet. (c) Results of amplification (final intensity value) for each set of primers (A, B or C) with or without the related RNA template in the sample test outlet (grey bars), with associated controls (positive: black bars; negative: white bars). (d) Picture of an unfolded longer wax geometry (multiplexed device), with dry amounts of dyes in the second last layer. Picture of the same device after folding and dipping into water: the dyes are conveyed to the top without mixing together. Picture of the same device, without dry components stored in it, fluorescein is pipetted in the middle spot simultaneously to the strip dipped in water. The yellow dye is distributed towards three sample tests outlets. (e) Schematics of the multiplexed paper device: exploded view and top view, and location of freeze-dried biological components (RT-RPA reagents with three different primers and associated RNA templates). (f) Normalized compared results of specific amplification of each template in the 9-outlet device (positive controls: black bars, negative controls: white bars; sample tests: grey bars).