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A transmission electron microscopy image has shown that the as-formed CoFe2O4 Co rods are composed of smaller nanocrystallines.
A transmission electron microscopy image has shown the flexible interleaved structure of nanocomposite, and the interface reaction is also benefit to ensure strong interfacial interaction between Fe3O4 nanoparticles (50 nm) and RGO nanosheets.
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Moreover, comparing mass spectrometry data with transmission electron microscopy images has enabled the mapping of subunits within topological models.
Note that length values in vitro and in silico are not comparable – the FilaQuant software processing florescence microscopy images has cutoff parameters (regarding length and thickness of lines to consider a filament) while for the simulation every integrin/focal adhesion with at least one bound actin is considered a filament.
Atomic force microscopy images have been obtained and Fourier transform infrared spectroscopy has been carried out to ensure that the AlN composition is maintained.
The texture degrees of carbon planes extracted from the experimental selected-area electron diffraction patterns as well as size of coherent domains extracted from high resolution transmission electron microscopy images have been used as reference points for modeling of material properties.
Transmission electron microscopy images have been obtained to know the structural configuration of the resulting molecules.
To the best of our knowledge, three methods for automated dendritic spine analysis from light microscopy images have been reported in the literature, only one of which operates on 3D data.
Interestingly, and in accordance with this, recent cryogenic electron microscopy images have revealed discontinuous structures of actin in filopodia which could more easily favor a bent structure and lower the bending energy.
As demonstrated in this work and earlier by others (see below), methods based on autocorrelation function (ACF) and spectral analysis of microscopy images have several drawbacks that preclude their use in the real-time estimation of sarcomere length for feedback control of the contraction where the accuracy of control input such as the sarcomere length is of importance.
In a first step fluorescence microscopy images have been collected to determine the relative fluorescence of specific domains in the sliced FCC catalyst particles, followed by a detailed TEM analysis of the ultra-structures, which show (in different degrees) fluorescence upon staining, or simply are not fluorescent.
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