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. 2023 Apr 7;23(11):2586–2600. doi: 10.1039/d2lc01113a

Fig. 6. Brightfield micrographs (A, B, G, H and I) showing cells captured in the DEP-BPE platform during a spike-in experiment. SK-MEL-28 cells spiked into healthy PBMCs were introduced at 100 nL min−1 under an applied voltage of 16 Vpp at 50 kHz. After 2 h, the cells were labeled on chip. Fluorescence micrographs show captured SK-MEL-28 cells in (C and J) yellow (MCAM), (E and K) red (MCSP), (F and L) blue (Hoechst nuclear stain), and (D) green (CD45) channels. (I) Is a higher magnification brightfield image of an individually captured SK-MEL-28 cell. The scale bars in (A, B, G and H) are 100 μm and in (C–F) and (I–L) are 20 μm.

Fig. 6