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. Author manuscript; available in PMC: 2020 Jan 15.
Published in final edited form as: Sens Actuators B Chem. 2018 Oct 4;279:447–457. doi: 10.1016/j.snb.2018.09.121

Figure 6. MERCA analysis of miRNAs in exosomes.

Figure 6.

(A, B) Background-subtracted fluorescence readouts for the detection of let-7a and miR-21 in a serial dilution of exosome standards derived from A549 (A) and U87MG cells (B). The concentrations of A549 and U87MG exosome standards were 2 × 1011 and 1 × 1010 vesicles/mL, respectively. Exosomes were lysed and then diluted by the TET buffer. 10 μL of each diluted sample was injected into the chip for analysis. Error bars are one standard deviation (n = 4). (C, D) Plots of the let-7a and miR-21 amount in A549 exosomes (C) and U87MG exosomes (D) calculated from the fluorescence readouts in (A, B) using the calibration curves in Figures 4 and 5, respectively. Error bars indicate standard error. (E) Bar graphs comparing the concentrations of let-7a and miR-21 in the original A549 and U87MG exosome standards measured by the MERCA and RT-qPCR. Error bars are one standard deviation (n ≥ 3). (F) Averaged miRNA copy number per exosome for let-7a and miR-21 in the A549 and U87MG exosomes, respectively, calculated from the MERCA results in (E).