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The morphologies were imaged using scanning electron microscopy (SEM) and transmission electron microscopy (TEM).
The chemical structures were characterized by Fourier transform infrared, 1H-NMR, 13C-NMR, mass spectra, whereas the morphologies were imaged using scanning electron microscopy and transmission electron microscopy.
Then, the samples were sputter-coated with gold and the porous morphologies were imaged at 20 kV acceleration voltage and 100 × magnification on a scanning electron microscope (VEGA3 TESCAN, Czech Republic).
Furthermore, detailed membrane morphologies were imaged with cryo-electron microscopy before and after Ca2+-injection.
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Calcium carbonate minerals and biofilm morphology were imaged in PAO1-gfp.
Texture and grain morphology were imaged using a TESCAN Vega2 scanning electron microscope (SEM).
Proximal and distal aortic areas with normal vessel morphology were imaged and showed no overall increase in diameter (data not shown).
Intensity of fluorescence was described in arbitrary units (AU) covering a range from 0 to 60 000 AU. Ca2+ levels and cell morphology were imaged every 10 min for 2 h using an Argon/UV laser (excitation 488 nm/emission 520 nm).
Morphology was imaged by optical microscopy.
The cell morphology was imaged and assessed via quantification of circularity.
Moreover, their surface morphology was imaged by atomic force microscopy and scanning electron microscopy.
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