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Cells attached to arsenopyrite coupons were visualized by staining with DAPI and were viewed using an epifluores-cence microscope.
Cultures were viewed using an inverted microscope to assess the degree of confluence and the absence of bacterial and fungal contamination.
The H&E staining technique was used to stain the slides, and they were viewed using an optical microscope (Olympus FSX-100, Olympus Corporation, Shinjiku-ku, Tokyo, Japan).
The slides were viewed using an epifluorescence Leica DMI 4000B microscope (Leica Microsystems Ltd., Hong Kong, China) equipped with a fluorescein filter.
Cilia were viewed using an inverted microscope (Diphot; Nikon, UK).
Slides were viewed using an Olympus Upright fluorescence microscope (BX61) and images were analyzed using Volocity software (PerkinElmer, Waltham, MA).
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Samples were viewed using a Zeiss LSM 510 META confocal microscope with a Plan-Apochromat 163 and 100×/1.4 Oil DIC objective.
Slides were viewed using a Leica LEITZ DMRX epifluorecence microscope.
Samples were viewed using a field-emission scanning electron microscope (FE-SEM) (Carl Zeiss Auriga, Germany).
The specimens were viewed using a Tecnai G2 transmission electron microscopy at 75 keV.
Compounding the evidence for this idea, 55percentt of all viewed videos were viewed using a mobile device in 2014 and that number keeps growing.
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