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Fluorescence microscopy provides a powerful method to directly observe single enzymes moving along a DNA held in an extended conformation.
Fluorescence microscopy provides a comprehensive tool for investigating many of these aspects of drug delivery in single cells and whole tissue.
Synchrotron IR microscopy provides a useful adjunct to molecular biological methods and underground observatories in the ongoing assessment of the role of root soil microbe communication.
The in situ transmission electron microscopy provides a novel approach to uncover the dynamic deformation mechanisms in nanostructured materials, especially at the atomic scale.
Combining stereology and polarisation microscopy provides a good estimate of grain boundary areas in ice beads and in natural snow, with some limitations.
The structure from negative-stain electron microscopy provides a detailed snapshot of an intermediate state in EBV entry and highlights the potential for the triggering complex to bring the two membrane bilayers into proximity.
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Negative-stain electron microscopy provides an approximation of the variable positioning of the BC dimers relative to the CT core.
Confocal microscopy provides an opportunity to explore multiple facets of fluorescence in living coral, including the identification of different colors being simultaneously expressed and the spatial distribution of those pigments across fine spatial scales.
Electron microscopy provides an excellent tool for measuring crystallinity, morphology and elemental composition.
In vivo microscopy provides an alternative approach to assess these morphologic changes in vivo.
Our dispersion phase microscopy provides an additional intrinsic parameter that could prove to be valuable in distinguishing different types of biomaterials or for imaging the spatial inhomogeneity of thin biological samples.
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