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. 2017 Jan 20;13:127–137. doi: 10.3762/bjoc.13.16

Figure 2.

Figure 2

Confocal microscopy of HeLa cells after transfection with DNA2aD1–DNA3rD5 (row 1), DNA2rD1–DNA3aD8 (row 2), DNA2aD2–DNA3aD8 (row 3) and DNA2rD4–DNA3aD8 (row 4). The visualization was performed using a Leica TCS-SPE (DMi8) inverted microscope with an ACS APO 63×/1.30 oil objective. For DNA2aD1–DNA3rD5 λexc = 405 nm (UV laser), λem = 435–470 nm (blue) and 575–750 nm (yellow), for DNA2rD1–DNA3aD8 λexc = 405 nm (UV laser), λem = 415–550 nm (blue) and 575–750 nm (red), for DNA2aD2–DNA3aD8 λexc = 488 nm (argon ion laser), λem = 490–550 nm (green) and 550–675 nm (red), for DNA2rD4–DNA3aD8 λexc = 488 nm (argon ion laser), λem = 490–550 nm (green) and 675–800 nm (red), scale bar = 20 µm.