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Characteristic morphological changes of breast cancer MCF-7 cells were observed by Scanning Electron Microscope as displayed in Figures 10 and 11.
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As displayed in Figure 1(a), no difference in cell morphology could be found between cMSCs derived from wt or Egr-1−/− mice when observed under inverted-phase microscope.
Samples were imaged on a Zeiss Meta 510 confocal microscope and displayed as projections of 1-μm serial sections.
Larval muscles 6 7 were imaged in abdominal segment A3 on a Nikon PCM 2000 or Zeiss Meta 510 confocal microscope and were displayed as projections of 1-μm serial sections.
The other two visual questions had a microscope image displayed on a computer screen.
The facility houses scanning confocals, spinning disc confocals, a light sheet microscope, and a range of wide field microscopes — as well as a transmission electron microscope (TEM) and scanning electron microscope (SEM).
Invasive cells were manually counted in a fluorescence microscope, and results were displayed as a percentage of cells that crossed the membrane (invading cells) relative to miR-NC.
Examinations of cultured islets under an inverted microscope showed that they displayed a regular cellular structure.
In the electron microscope some mitotic fibroblasts displayed a normal RER, others an inflated RER.
Some chose the microscope as their instrument.
Undaunted, the Sister offered her defense of the microscope as the liberator of contemporary women.
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