eGFP expressing tumor cells in brain metastases and red fluorescent microspheres were detected by confocal microscopy using Olympus FV1000 MPE (Olympus, Center Valley, PA).
The position and integrity of the internalized GF nanoparticles were evaluated by confocal microscopy using 4,6-diamidine-2-phenylindole dihydrochoride (DAPI, blue) as a marker.
HL-1 cells were spontaneously depolarizing 38 days after scaffold formation, which was visualized by confocal microscopy using a calcium-sensitive dye.
In this study, we developed a standardized approach for quantitative analysis of scar collagen morphology by confocal microscopy using fractal dimension and lacunarity analysis.
Sections were imaged by confocal microscopy using optical sections with 488-nm argon, diode lasers.
Apoptotic nuclei were visualized by confocal microscopy using a Nikon Eclipse Te 2000-S microscope.
Embryos and cells were examined by confocal microscopy using an Olympus Fluoview 1000 laser scanning Confocal Microscope (Olympus, Canada).
The cells were imaged by confocal microscopy using the MRC600 image system (Bio-Rad, Hercules, CA, USA).
Stained proteins were visualized by confocal microscopy using a FluoView™ laser scanning epi-fluorescence Olympus FV1000 microscope.
Cells were analyzed by confocal microscopy, using a 63X oil immersion objective on an Olympus FV1000 confocal microscope.
Samples were mounted using Prolong Antifade (Invitrogen) and analyzed by confocal microscopy using an Olympus Fluoview 500 laser scanning confocal on an Olympus IX61 upright microscope.
