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. 2019 Sep 25;5(9):eaaw6499. doi: 10.1126/sciadv.aaw6499

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Copyright © 2019 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC).

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Fig. 2 — (A) Bright-field and fluorescence microscopy images of HNTs/FAM-siRIPK4 fluorescence at 6 hours after transfection. (B) Flow cytometry analysis of fluorescent cells: representative histograms (upper panels) and means ± SD (lower panels, from three independent experiments). FAM-siRIPK4, fluorescein-labeled siRNA targeting RIPK4. (C) Confocal laser scanning microscopy analysis of the distribution of HNTs/FAM-siRIPK4 in T24 bladder cancer. Fluorescein (green)–labeled siRIPK4. DAPI (4′,6-diamidino-2-phenylindole; blue) was used to stain cell nuclei.