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The chemical composition and the success of hydrolysis have been assessed through infrared spectroscopy, while scanning electron microscopy verified that the spherical shape and the size (∼50 100 nm) of the NPs are practically unaffected by the hydrolysis process.
Field-emission scanning electron microscopy and transmission electron microscopy verified that the Li2MnSiO4/C nanocomposites finally obtained from 0.1 mol L−1 sucrose solution were agglomerates of Li2MnSiO4 primary particles less than 100 nm in size, and that there are thin carbon layers partially formed on the surface of these agglomerates.
Indeed, electron microscopy verified that staurosporine-treated Wt cells, but not DKO cells, exhibited hallmarks of apoptosis including nuclear condensation with maintenance of plasma membrane integrity, while ionomycin induced a purely necrotic phenotype that showed rupture of the plasma membrane and dispersion of the nucleus, which was not seen in DKO cells.
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Transmission Electron Microscopy (TEM) verified that cells of E. coli Bl21 were present in the intercellular space (Figure 2C) and inside cortex cells (Figure 2D).
Transmission electron microscopy (TEM) verified that fibrils were still the predominant species present after a 2 h treatment with EGCG (Fig. 1B).
Scanning electron microscopy (SEM) images verified that the production of 4.5 µm thick TiB2 layers was feasible after boriding for an hour.
Scanning electron microscopy (SEM) images verified that, at the composition ratios studied, PLA was dispersed as spheres or islands inside the TPU matrix and that this phase morphology further influenced the scaffold's microstructure and surface roughness.
We used scanning transmission electron microscopy (STEM) to verify that the Drosophila NECD is indeed dimeric.
Using transmission electron microscopy (TEM), we verify that N-terminal labeling of Aβ40 with AMCA, TAMRA, and Hilyte-Fluor 488 tags does not prevent the formation of protofibrils and amyloid fibrils of various widths.
We further performed the electron microscopy to verify the state of these TH+ neuronal cells.
For some people, electron microscopy brings that world into clear view, making seemingly impossible to imagine objects come to life.
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Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com