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. 2015 Nov 30;15(12):29882–29892. doi: 10.3390/s151229773

Figure 5.

Figure 5

(A) Agarose gel electrophoresis diagram of asymmetric PCR products. From left to right: DL1002 marker, F. thunbergii (c1, c2 and c3), F. cirrhosa (b), respectively; (B) Differential pulse voltammograms of different PCR products exposed to Tris-HCl buffer blank control (a), and hybridized with F. cirrhosa (b), F. thunbergii (c1, c2 and c3). Inset: Histogram of pure peak current corresponding to F. cirrhosa (a) and different F. thunbergii (c1, c2 and c3).