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. 2017 Nov 27;12(11):e0188359. doi: 10.1371/journal.pone.0188359

Fig 4. Model system for the scanning confocal fluorescence microscopy.

Fig 4

Total intensity spectra and confocal fluorescence microscopy images of Eu(III)@LTA with ATTO467N in the PVA film following 465 nm excitation and Eu(III)@LTA with F18, MitoTracker Red, and ATTO467N in the PVA film following excitation at 465 nm or at 488 nm monitored through a green bandpass filter (539–556 nm) or a red bandpass filter (604–644 nm) of an Edmund Optics filter kit. The profiles of the diagonal lines (dotted) through the images are plotted beneath showing the pixel intensities.