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The inter-planar spacing in a high resolution transmission electron microscopy image is approximately 0.26 nm corresponding to (002) plane of the ZnO nanorod structure.
A cross-sectional microscopy image is exploited to obtain a two-dimensional phase map (i.e., Ni, YSZ and pore), of which two-point correlation functions are used to reconstruct a three-dimensional model microstructure.
Different modes of correlation are presented here: a feature identified on a light microscopy image is used to guide the cryo-ET investigation, and cryo-tomograms are correlated to light microscopy images.
Consequently, the determination of the 3-D structure from nanoparticles by the use of a single electron microscopy image is a current challenge, which has been accomplished so far only for very specific systems such as size-selected gold clusters [17] and thin layers of light-weight atoms [18].
The size of the microscopy image is about 700 µm by 1000 µm.
Within the SECM system, one line of the confocal microscopy image is rapidly acquired by measuring the spectral content of the remitted light using a high-speed spectrometer (broadband input) or a high-bandwidth photodetector (wavelength swept source input).
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The confocal laser scanning microscopy image was used to validate antibody immobilization and determine where it occurred (Fig. 4).
If possible, the microscopy image was taken with the full worm in one image, otherwise separate anterior and posterior worm images were taken and later combined via meshAB.
For example, a standard practice in microscopy images is to apply a Fast Fourier Transform FFTT).
The ultimate lateral resolution of the scanning Auger microscopy images is determined by this value.
Heterogeneous illumination of the field of view in light microscopy images is inversely related to objective magnification.
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