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After cleavage reaction, the separation of the 6FAM/Cy5-17DS 6FAM/Cy5-17DS by utilizing fluorescence microscopy (Nikon).
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Localization microscopy was also performed by utilizing fluorescence lifetime of conventional fluorescent dyes [ 17] or reversible photobleaching of conventional fluorescent proteins [ 18].
The thermal imaging of an active nucleation site was performed by utilizing high-resolution, fluorescence microscopy, which enabled a maximum spatial resolution of 370 nm/pixel.
Cells were either analysed by immunoblotting or by fluorescence microscopy.
The uptake of microparticles by CACs was determined by fluorescence-activated cell sorting and by fluorescence microscopy.
The DNA bundle and the intercalation results were preliminarily checked by scanning electron microscopy (SEM) and by fluorescence microscopy.
Nunes, P., Guido, D. & Demaurex, N. Measuring phagosome pH by ratiometric fluorescence microscopy.
Essentially all the cells expressed GFP by UV fluorescence microscopy (Figure 2b).
Cells were imaged by confocal fluorescence microscopy (LSM510 Meta, Carl Zeiss MicroImaging Inc., Tokyo, Japan).
The molecules were injected i.v. and the fluorescence in tumour tissue was quantified by intravital fluorescence microscopy.
Ca2+ levels were determined by a fluorescence microscopy.
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