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The photographs of wet, freeze-dried, and air-dried beads, taken under an optical microscope, are shown in Figure 1.
DF image from the agglomerate and diffractions before and after heating in the column of microscope are shown in the insets Fig. 5 Composite particles in Ni49.9Ti40.3Zr0.3Cu0.1Hf9.4 powder.
In Fig. 10, TEM micrographs of the grain boundary in focus (a c) as obtained with each microscope are shown as well as the finally calculated intensity derivatives (d f) and the corresponding reconstructed phase images (g i).
Images taken by a coupled charge camera device (CCD) connected to the inverted microscope are shown in Fig. 2. As a control experiment, the excitation of a bare and conjugated ZnO NRs was first performed.
Fluorescence images of freshly excised adenomas incubated with QPIHPNNM and GGGAGGGA collected with a bench top confocal microscope are shown in Fig. 4. The image of QPIHPNNM (Fig. 4a) demonstrates binding pattern of the target peptide to single epithelial cells, representing similar morphological features to that seen on microendoscopy.
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The surface morphology of treated mild steel examined by scanning electron microscope is shown in Fig. 10 for samples treated with 1N hydrochloric acid solution, Fig. 11 for samples treated with 1N sulfuric acid solution, and Fig. 12 for sample treated with HNO3 solution.
A photograph of the pressurized chamber on the stage of an Olympus IX71 inverted optical microscope is shown in Fig. S1A.
The cell surface as seen under the scanning electron microscope is shown in Figure 1A, to contrast with subsequent images of attached spirochetes.
The setting of the flowcell within the laser scanning confocal microscope is shown in Figure 1.
The distribution of the intracellular Fe granules observed under transmission electron microscope is shown in Figures 5 e)- 5(f).
The configuration for differential phase contrast combined with the X-ray microscope is shown in Fig. 1(a), where an X-ray Talbot interferometer [ 17] is located in front of the image detector [ 18].
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com