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. 2016 Aug 17;6:30245. doi: 10.1038/srep30245

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Copyright © 2016, The Author(s)

This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/

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Florescence microscopy of H23 cells incubated with TBN (Gel_FlAb-siRNA_Cy5) and its analogues Gel_FlAb-siRNA, Gel-Ab_Cy5-siRNA, Gel-Ab-siRNA_Cy5, siRNA_Cy5 and Ab_Cy5. DAPI was used as a nuclear staining marker. Fluorescein was used for encapsulation in Gelatin Nanoparticles. Cy5 was used for labelling antibody and siRNA. The figure shows co-localization of cy5 labelled siRNA and fluorescein encapsulated gelatin nanoparticles in H23 cells. Appropriate controls with and without fluorescein or cy5 were used. All images were recorded at 20X magnification.