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Using these methodologies, our data show that in human embryonic kidney 293 (HEK293) cells, CaM diffuses at a rate slower than expected on the basis of the molecular weight and cytoplasmic viscosity (10 μm/s), whereas enhanced green fluorescent protein (eGFP) diffuses at ∼20 μm/s.
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Before we get to that, though, a few words about our methodology: Our data was culled from the review aggregator Metacritic.
Within the limits of detection of this methodology, our data suggest that the RuvABC resolvase is able to act in the ΔrecG ΔclpX mutant and resolve a substantial proportion of the Holliday junctions tying the DNA linear molecules together.
In terms of methodology, all our data argue that the Dnmt1/PCNA Proximity-Ligation In Situ Assay presented here should enable to reflect the degree of DNA methylation in cells.
We otherwise faithfully applied the study's statistical methodology to our data, obtaining the correlation between where l indicates the time lag of l days between the averaged sunshine duration and day of suicide, and k the period of k days for which sunshine duration was averaged.
Differently from survey methodologies, our method affords data collection and behavior characterization at the individual level, and thus may be used to inform agent-based modeling approaches.
We first explain our methodology and then our data sources in the following two sections.
Therefore, before applying the methodology, we describe our data collection strategy.
This methodology ensures that our data are complete and correct and that the proportion of participants can thus be considered to be accurate.
Our data, methodologies and workflow will have to cut across different disciplines.
Our data, methodologies and approaches to tackle problems will have to cut across various disciplines.
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CEO of Professional Science Editing for Scientists @ prosciediting.com