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Scanning electron microscopy demonstrated the development of intercellular gaps.
Optical microscopy demonstrated the changes in the morphology of K562 cells in different experimental conditions.
Upper panels (A1 A6): image of 20× microscopy demonstrated the healthy morphology of neurons.
Atomic force microscopy demonstrated the perfect uniformity and planarity of the cured films.
Furthermore, atomic force microscopy demonstrated the formation of PLLA nanobrushes on the pSi surface.
Immunofluorescent confocal microscopy demonstrated the recombinant TAT-fusion proteins with a mixed endosomal and lysosomal localization.
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The analysis of the surface by electron microscopy demonstrates the absence of surface attack patterns in the presence of the oil.
Lattice imaging by high-resolution transmission electron microscopy demonstrates the characteristic MAX-phase stacking of α-Ta4AlC3.
Characterization of prototype alloys by transmission and analytical electron microscopy demonstrates the precipitation of B2 or L21 aluminide in a (Nb) matrix.
The growth and differentiation of individual cell types was determined using live cell fluorescent microscopy demonstrating the utility of fluorescent labels to monitor tissue organization in real time.
Characterization by x-ray photoelectron spectroscopy, x-ray diffraction, and transmission electron microscopy demonstrates the high purity, perfect stoichiometry, and nanocrystalline structure of both layers.
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CEO of Professional Science Editing for Scientists @ prosciediting.com