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Cross-section microscopy has proven to be highly complementary with MA-XRF, combining the overall compositional information of a painting with local, but layer specific analysis of a paint system on the microscale [5].
THG microscopy has proven effective for studying cell divisions in the early zebrafish embryo [ 5].
One technique, Laurdan fluorescence microscopy, has proven very useful for distinguishing such regions but has hitherto relied on 2-photon confocal microscopy.
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As graphene is replete with unique structural and electronic properties scanning probe microscopy has proved to be an exciting and a rewarding venture.
In physiological systems, Laurdan microscopy has proved its usefulness in showing distinct clustering of Caveolin-1 with membrane domains of increased order [34] and has shown the increased order of the lamellopodia of macrophages [35] compared to other regions of the cell's membrane.
This configuration is known in X-ray microscopy and has proven to be useful, but has not been applied to neutral atom beams.
To find out more about the mechanisms of bacterial adhesion, atomic force microscopy (AFM) has proven to be the tool of preference in order to determine the forces by which bacteria attach to surfaces and keep themselves adhered (Dufrene 2002; Dorobantu and Gray 2010; Müller and Dufrêne 2011; Dorobantu et al. 2012).
Recent SSF experiments with an initial dry-matter content of 27% (w/w) have produced ethanol levels of over 60 g/kg slurry [ 18] Atomic force microscopy (AFM) has proven to be a powerful tool for visualising the surface of plant cell walls [ 19- 22] including modification of plant fibres and pulp [ 23- 25].
The successful creation of a composite hydrogel using MDP fibers and labeled GF loaded liposomes, as determined by electron microscopy and rheology, has proven that orthogonal self-assembly of multiple components within a single system is a competent approach toward formation of novel and more complex architectures able to mimic naturally existing ones.
Fluorescence light sheet microscopy, such as selective plane illumination microscopy (SPIM; Huisken et al., 2004), has proven to be a powerful tool to image developmental processes in vivo with fast, high-resolution optical sectioning over large volumes (Huisken and Stainier, 2009).
Serial block-face scanning electron microscopy (SBEM) has proved to be a remarkable technique for imaging at moderate lateral and axial resolution (approximately 10 and 40 nm, respectively) and across large fields of view spanning many hundreds of microns of sample.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com