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Therefore, dynamic monitoring of cell adhesion and FA formation could be achieved by fluorescent microscopy utilizing the automated microscopy system Hermes Wiscan.
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Entire detached inoculated leaves were then observed by fluorescent microscopy 24 hpi and fluorescence emission was evaluated for each condition.
Fluorescence signals were analyzed by fluorescent microscopy (Nikon, Tokyo, Japan).
For all infections, a cloned line of Plasmodium berghei ANKA (Pb ANKA) strain stably transfected with the green fluorescent protein (GFP) on hsp70 promoter [51], was utilized allowing the detection of sporozoites and blood stage parasites by fluorescent microscopy.
Other genetic approaches utilize systemic tagging of yeast genes and determining the localization of the fusion proteins by fluorescent microscopy.
All these results were confirmed by fluorescent microscopy micrographs after calcein/ethidium staining (Fig. 2C).
BrdU and CD31 staining in GC muscles was analyzed by fluorescent microscopy.
Sample purity was confirmed by fluorescent microscopy (see Supplementary Figure 2C).
This strategy allowed them to visualize these lymphatic systems by fluorescent microscopy.
Intercellular Ca2+ signaling was monitored by fluorescent microscopy.
EGFP expression was localized in vivo by fluorescent microscopy and fluorescent laparoscopy.
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