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MRI images of control rats of the same age were coregistered with those of lesioned rats.
(A) Representative BF images of control and ASPM-2 organoids at different stages.
Fig. 2 SEM images of control and ethanol-stressed I. orientalis cells.
Fig. 5 Fluorescence microscopic images of control U937 (a), K562 (c), GNP-NKCT1 treated U937 (b), treated K562 (d) cell line.
Confocal microscopic images of control U937 (e and i), K562 (g and k) and GNP-NKCT1 treated U937 (f and j), treated K562 (h and l) cell lines.
Fig 7 Cell uptake study (a c LSCM images of FITC-csMSN, d, e TEM images of control group and csMSN group).
After the biofilm formation, the AFM images of control samples indicated prominent and integrated biofilm surface topology of both the tested bacterial strains, i.e. S. aureus, S. mutans (Figs. 6a, 7a respectively).
Fluorescence images of control A549 cells (without silver nanoparticles (AgNPs)) and cells treated with biologically synthesized AgNPs (bio-AgNPs) (25 μg/ml) and chemically synthesized AgNPs (chem-AgNPs) (70 μg/ml).
Fluorescence images of control A549 cells and L132 cells (without silver nanoparticles (AgNPs)) and cells treated with AgNPs (30 μg/ml).The changes of mitochondrial membrane potential by AgNPs were obtained using fluorescence microscopy.
Representative images of control and SM-Dicer KO aortae are shown in figure 4E.
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15 Automated and manual counting was performed using 10 high quality images of controls at 5° retinal eccentricity, with a central sampling area 300×300 px (equal to the central 240×240 μm).
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