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Microscopic observations were carried out under an epifluorescence microscope (AxioPlan 2 Imaging System, Carl Zeiss, Jena, Germany).
The cells were enumerated using an epifluorescence microscope (Nikon 80I) at 1000×.
At 72 hpi, the cells were observed using an epifluorescence microscope to visualize the expression of EGFP.
The intracellular lipids were examined by using an Epifluorescence Microscope (Nikon DS-Ri1) at the wavelength of 540 nm.
Images were taken by a CCD camera attached to an epifluorescence microscope (Axioskop 2, Carl Zeiss AG, Germany).
The slides were observed under an epifluorescence microscope (Nikon, Eclipse 80i, Kanagawa, Japan) at ×200 and ×400 magnification.
The sections were examined in an epifluorescence microscope (Nikon 80i, Tokyo, Japan) equipped with a Nikon DS-2MV camera.
High-resolution microscopic examination of the same tissues could be done by a relatively inexpensive modification of an epifluorescence microscope using a custom designed diode laser light source.
Here, we prepared liposomes that were partially stained with a fluorescent dye, and analyzed their fluorescence intensity under an epifluorescence microscope.
Images were collected on an epifluorescence microscope.
Cells were analyzed using an epifluorescence microscope (Nikon, Melville, NY).
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