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Since hemocytes are adherent and can be visualized through the cuticle by fluorescence microscopy, we followed their localization in vivo after CrPV injection.
Using automated time-lapse fluorescence microscopy we followed dynamics of Trx-CFP and TrxR1-YFP in individual cells upon addition of 10 µM CPT to the cell medium.
Using time-lapse video microscopy, we followed the trans-localization of TbCPC1-EYFP and were able to fully confirm our previous conclusion [11].
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Using time-lapse video-microscopy we followed the migration of serum-starved PC-3 cells in co-culture with BMS containing D8-AA-loaded adipocytes.
To select for S phase cells, we followed cells live by microscopy and screened the RFP signal.
Following immuno-electron microscopy we detect SmAQP by immunogold labeling and observe gold particles often clustered in the parasite tegument.
Again, we imaged cells with two photon time lapse microscopy and followed it with post hoc immunohistochemistry (Fig. 5A E, E1).
Here we compared different chloroplast structures by confocal laser scanning microscopy (CLSM) followed by computer modeling and by transmission electron microscopy (TEM).
Here, we present a system for single-cell lysis under light microscopy observation, followed by rapid uptake of the cell lysate.
We found that using a loop to transfer lipid monolayer crystals to an electron microscopy grid followed by embedding in trehalose and quick-freezing in liquid ethane also yielded the highest resolution images for sbpA lipid monolayer crystals.
We investigated actin cytoskeleton architecture in dependence on defined surface topography with confocal laser scanning microscopy subsequently followed by the quantification of actin filament formation via the software FilaQuant.
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