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SiNWs morphologies are checked by scanning electron microscopy (SEM) before and after electrochemical cycling.
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After reconstruction, morphologies were checked for accurate reconstruction in x/ y/ z planes, dendritic diameter, and no unconnected dendrites.
The morphology was checked by means of transmission electron microscopy.
X-ray photoelectron spectroscopy (XPS) and ATR-FTIR (Attenuated Total Reflection Fourier-Transformed Infrared) spectroscopy were used to study the bulk and surface chemical composition of the films, X-ray Diffraction (XRD) analysis allowed lattice structure and grain size determination while samples morphology was checked with a scanning electron microscope (SEM).
The kidney morphology was checked by HE staining.
Embryo morphology was checked on days 2 and 3 using the scoring system reported elsewhere [ 40].
After 60 hr, the PVD morphology was checked at the young adult stage.
The cell morphology was checked at the different time points during the culture period using light microscopy.
All cell lines are routinely tested for mycoplasma using a PCR-based method, and the morphology is checked visually by microscope.
All experiments were performed independently in triplicate and data were presented as mean ± S.E.M. Changes in cell morphology were checked visually under phase contrast microscope (Carl Zeiss Axiovert 40 CFL, Germany) after incubation with IC50 concentrations of TAFU for 24, 72 h, where untreated cells served as control.
The change in the surface composition and morphology has been checked by XPS, AES and AFM data.
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