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54 protocols using s 800

1

Worn Surface Analysis of Specimens

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The worn surfaces of a representative specimen in each group after 40,000 cycles were observed using a scanning electron microscope (SEM, S-800, Hitachi Corp., Tokyo, Japan) at ×40 and ×5,000 magnification.
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Scanning Electron Microscopy Analysis of Cells

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For scanning electron microscopy (SEM) analysis, the specimens were fixed in phosphate-buffered saline containing 2% glutaraldehyde and 0.1% paraformaldehyde for 2 h. Then, they were stained with 1% OsO4. Specimens were coated with gold using an EiKO IB-3 ion sputter coater (EiKO, Shawnee, KS, USA) and examined with a field emission gun (FEG) scanning electron microscope (S-800, Hitachi, Japan) at an acceleration voltage of 20 kV. Images were processed with ESCAN 4000 software (Bummi Universe Co., Ltd., Seoul, Korea). For cell length measurements, more than 100 straight-lined cells were chosen randomly from digitized SEM images, and the distance between the two poles of each cell was automatically calculated.
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3

Comprehensive Characterization of Coated SPIONs

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The morphology of all investigated uncoated and coated SPIONs was determined by scanning electron microscopy (SEM-JEOL, JXA-840A Electron Probe Micro-Analyzer, Japan). Energy-dispersive X-ray (EDX) spectroscopy was applied on an SEM-field emission microscope (Hitachi S-800, Oxford, USA) to assess the atomic concentration of various elements on the top surface of the considered samples. Confirmation of the nanostructure was performed using a transmission electron microscope (TEM, JEOL, Japan). X-ray diffraction analysis was used to determine the crystalline phases of the magnetite and their coated nanoparticles using a Bruker diffractometer (Bruker D8 advance, Germany). The patterns were run with a CuKa1 target with a second monochromator 40 kV, 40 mA. The molecular structure was studied qualitatively using a Fourier transform infrared spectroscopy (FTIR) (6100 JASCO) in the range of 4000–400 cm−1. A vibrating sample magnetometer (VSM), (LakeShore 7400; Chicago, IL, USA) was used to investigate the magnetic properties of the magnetite nanoparticles at 300K.
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4

Characterization of GHPA Hydrogel Morphology

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The morphology of the GHPA hydrogels was examined by SEM (S-800, Hitachi, Tokyo, Japan). The GHPA hydrogels were prepared in a cell culture slide (SPL life science, Gyeonggi-do, Korea) by mixing 100 μL of 3 % GHPA containing HRP (0.005 mg/mL) and H2O2 (0.01 wt. %). The cross-linked hydrogels were freeze-dried over a 2 day period. The dehydrated hydrogels were sputter coated with an ultrathin layer of gold/platinum by ion sputtering (E1010, Hitach, Tokyo, Japan) prior to the SEM observations.
Compositional analysis of the GHPA hydrogel was performed by FT-IR spectroscopy (Nicolet 560, Nicolet Co., Madison, WI). The GHPA hydrogel was prepared on a slide glass covered with cover glass.
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5

Microscopy Imaging and Bristle Counting

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Images of embryonic legs were captured under bright-field illumination by using a Zeiss AxioObserver Z1 inverted microscope. Images of nymphal and adult legs were captured by using a Hitachi S800 scanning electron microscopy. Bristles were manually counted using the tool PointPicker implemented in Fiji (54 (link)).
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6

Scanning Electron Microscopy of Wheat Starch

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The surface of wheat starch granules was observed using scanning electron microscopy (SEM). The analysis was carried out as described by Hung and Morita (2005). A certain amount of starch was suspended in 95% ethanol for a few minutes and then sprinkled onto a double-sided adhesive tape mounted on an aluminum stub. After being dried by vacuum aspiration for several hours, the samples were coated with Pt/Pd and photographed using an SEM apparatus (Hitachi model S-800, Tokyo, Japan) at an accelerating potential of 10 kV [24 (link)].
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7

Catalyst Surface Morphology by SEM

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Scanning Electron Microscopy (SEM) Hitachi S-800 instrument was used to image the catalyst surface to determine morphological characteristics.
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8

Analyzing Composite Morphology via SEM

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The morphology of the composites was evaluated using scanning electron microscopy on the surface and longitudinal and transverse cross-sections. The composites were cut along the longitudinal or transverse axis with a scalpel, hydrated in sterile PBS, dried in a critical point dryer, sputter-coated with gold, and then observed with a scanning electron microscope (Hitachi S-800, Tokyo, Japan) (Scott et al., 2011).
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9

Biofilm Assay with Duck Serum

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The biofilm assay (1% crystal violet method) was performed as previously described in 96-well plates with duck serum6 (link), and A595 was recorded. Wells with the DH5α strain cultured in 50% sterile duck serum served as controls. All biofilm assays were run in triplicate. SEM was performed as previously described6 (link). Observations were performed at 15 kV with a scanning electron microscope (model S800; Hitachi, Tokyo, Japan).
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10

Morphological Changes in Egg Protein Powder

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The change in morphology of egg protein powder after desalting was examined by scanning electron microscope (Hitachi S-800, Hitachi Co. Ltd., Tokyo, Japan). After fixing with 2.5% glutaraldehyde for 2 h, the samples were washed with distilled water for 5 min. After dehydrating in a graded ethanol series for 30 min (five steps of 10% increments, starting with 60% ethanol), the samples were observed using a gaseous secondary electron detector at a voltage of 10 kV.
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