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Correlative fluorescence and electron microscopy has become an indispensible tool for research in cell biology.
Fluorescence nanoscopy, or super-resolution microscopy, has become an important tool in cell biological research.
Modern light microscopy has become a most powerful analytical tool for studying molecular processes in live cells.
The synergy between X-ray crystallography and cellular fluorescence microscopy has become particularly important, precisely because the results from these two methods diverged and highlighted the complexity of the challenge.
Total internal reflection fluorescence (TIRF) microscopy has become the technique of choice for imaging the regions of cells in closest apposition to the substrate surface.
With advances in spatial resolution reaching the atomic scale, two-dimensional (2D) and 3D imaging in electron microscopy has become an essential methodology in various fields of study.
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Scanning fluorescence microscopy techniques such as confocal [ 1] and two-photon [ 2] microscopy have become indispensable tools in the biomedical community.
Scanning transmission electron microscopy (STEM) has become one of the fundamental tools to characterize oxide interfaces and superlattices.
Over the past two decades atomic force microscopy (AFM) has become one of the most frequently used tools for studying polymer crystallization.
Scanning tunneling microscopy (STM) has become established as a versatile technique for direct, real-space investigations and characterization of matter at the atomic level.
Three-dimensional (3D) electron microscopy (EM) has become a major player in structural cell biology as it enables the analysis of subcellular architecture at an unprecedented level of detail.
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