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This approach normalizes the ROS upregulation with respect to the number of viable cells at the time of measurement.
To study the integrity of the FSH receptor (FSHR) signaling pathway in granulosa-lutein cells at the time of egg retrieval and its relationship with the infertility diagnosis.
The MTT assay was done on both heat-treated and untreated cells at the time points of 0, 124 248 48, 78, 96 and 105 h of dark cultivation.
DPI, added to the cells at the time of maximum FMLP-activated membrane depolarisation, accelerated the rates of both membrane repolarisation and influx of Ca2+, while KB-R7943 effectively antagonised these processes.
All recipients that were pretreated with the intrathymic plus GK1.5 and that were injected with naive 2C cells at the time of heart transplantation experienced rejection of the BALB/c (Ld+), but not the dm2 (Ld–) hearts.
The number of samples included in each assay varied based on the availability of cells at the time of testing.
Another reason for the discrepancy could be differences in the growth rate of the cells at the time of lysis.
We analyzed five relatively short filaments, starting from 16 24 cells at the time of nitrogen step-down.
When doxycycline induction is initiated in detached cells at the time of plating, cells fail to adhere.
These longer delays are clearly due to decreasing fractions of viable cells at the time of inolucum.
Two recently published studies suggest that the age of the labeled cells at the time of learning is critical in determining the effects [30], [31].
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com