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The fabricated scaffolds using freeze-dry technique were used as a 3D model to monitor cell proliferation and migration.
Furthermore, the integration of the designed microsystem with the multi-well plate reader allowed to monitor cell proliferation in situ during the cultures.
To determine if the difference in cellular iron levels between cell lines is due to differential release into the medium, M17, PrPC, PrPΔ51 89, PrPΔ23 89, and PrP102L cells were cultured in the presence of 3H-thymidine overnight to monitor cell proliferation and radiolabeled with 59FeCl3 for 4 hours as above.
We also employed the crystal violet staining assay to monitor cell proliferation.
Next, the optimal drug concentration was determined to monitor cell proliferation.
During this time, the real-time cell electronic sensing system was used to monitor cell proliferation.
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Case studies are presented describing the use of cell‐based imaging assays for monitoring cell proliferation, cell cycle stage, and apoptosis.
After 120 h of monitoring cell proliferation with this System, we observed a continuous decrease of cell growth and motility in both miR-875 transfected cells and miR-3144 transfecellscells.
We next introduced Zfp277 deletion mutants into Zfp277−/− MEFs and monitored cell proliferation.
We used an immunocytochemical system for monitoring cell proliferation using monoclonal anti-5-bromo-2'-deoxyuridine (BrdU) to detect BrdU incorporation into cellular DNA.
MTS is a very common method for monitoring cell proliferation, and is useful because it specifically detects viable cells, in contrast to many other labeling protocols that do not discriminate between live and dead cells.
More suggestions(15)
monitor cell line
monitor cell uptake
monitor cell microenvironment
monitor cell state
monitor cell respiration
monitor cell size
monitor cell responsiveness
monitor cell fate
monitor cell density
monitor cell cycle
monitor cell index
monitor cell biology
monitor cell phone
monitor cell repair
monitor cell membrane
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