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The cells were imaged using a confocal laser scanning microscopy.
Fluorescence was observed using a confocal laser scanning microscope.
The fluorescence was then visualized using a confocal laser scanning microscope (LSM710, Zeiss, Germany).
Images were acquired using a confocal laser microscope (Eclipse TE 2000, Nikon Corporation, Tokyo, Japan).
Samples were analyzed using a confocal laser scanning microscope (CLSM; Zeiss, model LMS700, Germany).
The intracellular distribution of DOX was also studied using a confocal laser scanning microscope.
Images of visual cortex were obtained from tissue slices using a confocal laser scanning microscope.
Finally, the cells were observed using a confocal laser scanning microscope (Fluoview FV-1000, Optical OptiCo. Co., Ltd., Tokyo, Japan).
Slides were analyzed using a confocal laser scanning microscopy (Zeiss, LSM 510 UV, Jena, Germany).
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Chlorophyll imaging was carried out using a confocal laser-scanning microscope (μRadiance; Bio-Rad Laboratories InCA, HercUSAs, CA, USA).
Microscopic analysis was performed using a confocal laser-scanning microscope (Zeiss LSM 710 META, Germany).
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