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ER microsome-targeted RNCs in membrane buffer were divided into two equal portions (10 μl each) and incubated with either 200 μM N-ethylmaleimide (NEM, Sigma Aldrich) or an equal volume of DMSO for 1 hr at 0°C.
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Thus, a buffer is divided into five message spaces.
This buffer is divided into different lengths, such as N/4,N/8,N/16… to store one row of LL coefficients.
The third side(if the buffer is divided into for sides) is for brushing away ridges from the nail, and the forth side, glosses the nail by bringing the oil to the surface, This makes the nail shiny, plus, allows nail polish to stay on longer.
Rank scores for these items were combined for each buffer, and buffers were divided into low, medium, and high tertiles of SES based on overall rank scores, as per existing precedents [ 47, 48].
The percentage of total land within each buffer that consisted of total natural space, green space, and blue space was estimated, and the buffers were divided into equal quartiles based upon the distribution of values for each measure.
To compare the relative content of pCofilin or Cofilin in synaptoneurosomes, each sample from a single animal was homogenized in ice-cold homogenization buffer A, and the homogenates were divided into 2 aliquots.
To facilitate the penetration of staining buffer, plants were cut into segments of approximately 10 mm, and large calli were divided into several pieces.
Aortic rings were divided into 5 groups: intact, denuded, l-NAME pretreatment, MB pretreatment, and Ca2+-free Krebs buffer.
"We were divided into groups.
The guests were divided into teams.
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CEO of Professional Science Editing for Scientists @ prosciediting.com