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In the absence of ATc, proliferating parasites were not noted in the cultures examined using an inverted microscope to monitor tissue cultures.
The glomeruli were incubated at 37°C for 10 15 min. During incubation, the glomeruli were triturated every five min. A portion of the sample was observed under a microscope to monitor cell dissociation.
To investigate the role of CD4+CD25+ regulatory T cells in the pathogenesis of silica-induced lung fibrosis, the lung tissues of mice were observed by light microscope to monitor pathological changes and graded for silicotic nodule (Table 1).
Bight-field images were taken using the transmitted light channel in a Zeiss LSM 510 META confocal microscope to monitor the early visible phenotypic effects of defensins on conidial germination and growth of fungal hyphae (at 16 hours after treatment with defensins).
We prepared and stained the acute slices of SCN with a bath application of 20 µM fluo-4 AM (Fig. 1A and B) as described in Materials and Methods, and used a laser-scanning confocal microscope to monitor their short-term [Ca2+]c activities over a duration of 800 seconds.
The top was then imaged using a fluorescence microscope to monitor accumulation of particles.
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The microstructures of such coatings were analyzed herein using an optical microscope (OM) and scanning electron microscope (SEM) to monitor the morphologies of both powders and coatings of Fe-based alloy.
Cells in cytokinesis or early in G1 were incubated for 24 h in a 5% CO2-equilibrated chamber maintained at 36.5 37°C on the microscope stage to monitor the plasmids throughout a cell cycle.
In these experiments, a confocal microscope was used to monitor the fluorescence intensity in a small region of interest (ROI) within the nucleus or cytoplasm before and after irreversibly photobleaching the molecules within the ROI by repetitively scanning at 100% laser power.
Every week, embryogenesis cultures, were observed under a microscope Leica MZ16FA, to monitor the embryogenesis process.
"Current technology with laser scanners and microscopes allows us to monitor retinal diseases at the microscopic level, but the things we see are beyond the physiological limit of what the human hand can operate on.
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