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. 2015 Aug 7;10(8):e0134957. doi: 10.1371/journal.pone.0134957

Fig 4. Subcellular localisation of SA43 and SA44 with endoplasmic reticulum (ER), golgi apparatus (GA) and lysosomes.

Fig 4

Live U87MG cells were incubated separately with Cy3 labelled SA43, SA44 and RA at a concentration of 100 nM for 24 hours. CellLight ER and GA labelled with GFP, and lysotracker green DND-26 were then incubated to the cells to track the co-localisation of aptamers with ER, GA and lysosomes respectively, and fixed using 4% PFA. The nuclei were counterstained with DAPI (blue). Cells with random aptamer and marker alone were used as control. Bar = 10 μm.