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By means of sliding wear and torsional fatigue tests followed by electron microscopy, it is shown that austenitic materials generate wear particles of either nano- or of microsize.
In vibrational microscopy, it is often necessary to distinguish between chemically distinct microscopic objects and to highlight the "chemical interfaces" present in the sample under investigation.
By means of scanning tunneling microscopy, it is observed that molecules of the form n-alkylcyanobiphenyl, where n = 8 to 12, form two-dimensional crystalline domains when adsorbed onto graphite.
Thanks to Transmission Electron Microscopy, it is shown that chlorine or fluorine incorporation promotes the formation of the same neutral defects, which are {011} cassiterite twins.
Unlike other analytical techniques, e.g. based on electron microscopy, it is not limited to surface characterisation or thin sections, but rather allows non-destructive measurements in the material bulk.
Furthermore, using confocal laser scanning microscopy, it is demonstrated that fluorescently labeled lysozyme is not only adsorbed to the negatively charged particles' surface, but also diffusing into the matrix of eADF4(C16) particles.
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Third, using confocal microscopy it was found that GdBN co-localise with lysosomes but not with mitochondria.
From scanning electron microscopy, it was found that connection between MgB2 grains and voids strongly depend on the growth temperature.
By fluorescence microscopy, it was observed that the nanoparticles were not located homogeneously on the cells and on the membrane (Figure 5).
After examination under SEM and light microscopy, it was revealed that the number of cells decreased in the presence of pure Mg, Mg10Gd and WE43.
By means of immuno-electron microscopy, it was shown that MMP-9 associates with hippocampal dendritic spines bearing asymmetrical (excitatory) synapses.
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