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A scanning electron microscope survey was initiated to determine if the previously reported findings of "dinosaurian soft tissues" could be identified in situ within the bones.
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Microscope slides were also surveyed for cells in rare life cycle stages.
The scanning SQUID microscope system at the Geological Survey of Japan (GSJ), AIST, is shown in Fig. 1.
Cells that invaded the lower surface of the filters were surveyed under a microscope at 100× magnification, and five fields were randomly selected.
Cells that migrated to the lower surface of the chambers were surveyed under a microscope at 100× magnification, and five fields were randomly selected.
The morphology, particle sizes and elemental composition of the prepared adsorbents were surveyed using a scanning electron microscope coupled with energy dispersive X-ray spectrometer (SEM-EDAX, HITACHI S-300 N).
Each vaginal sample was rehydrated with normal saline solution and surveyed under a phase contrast microscope with 400× magnification and an area of 0.016 mm.
The use of simulations allows for a systematic survey of a range of materials and microscope parameters to inform optimal experimental design.
After 48 72 hours incubation at 37°C, infection events reflected by fluorescent cells (expressing the marker plasmid) were determined by surveying the whole well in a fluorescence microscope and/or by flow cytometry (min. 5×104 cells acquired).
Beginning either 50 hours (20°C) or 30 hours (25°C) after L1 stage, nematodes were surveyed hourly for eggs using a dissecting microscope.
The cells were kept in the flasks surveyed by photographing in an inverted phase-contrast microscope repeatedly during up to 3 or 4 weeks after irradiation.
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