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The paired-samples t-test was used to assay the differences in the miRNA expression levels between cancer tissues and corresponding adjacent tissues.
In this context it is important to note that although activation of these four Cup systems results in a similar phenotype in an in vitro biofilm assay, the differences in regulation and organization would suggest that they are not redundant.
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Like the lifespan and fecundity assays, the differences among lines in resistance to oxidative stress suggests allelism, as variation in the wild-type background was not greater than variation in the mutant backgrounds (Table 3).
As similar concentration of fibrillar BSA-Zwit and BSA-S200 was used in the cytotoxic assay, the difference in potency is likely due to factor(s) other than concentration of amyloid fibrils.
In the case of the cytotoxicity effect of Maldi 531.2[M + H] + as shown in cell viability tests and annexin V-FITC binding assay, the difference in IC50 values with XTT at 0.02-0.03 uM and the non-significant difference of cytotoxic effect at 0.05 uM with annexin V FITC binding assay for apoptosis, relative to untreated cells, is the time of observation.
With both MN assays the differences in proportion of radiosensitive patients and controls were significant (chi-square test, Table 1).
2) In contrast to the binding assays, the actual differences in relative survival of N. meningitidis in the presence and absence of CFHR3 are rather modest.
Excluding these nine assays, the difference in the proportion of 'true' indeterminate results between the two assays was not statistically significant (3/96 vs. 5/87, p = 0.48).
We developed a multiplexed SRM assay to verify the differences in protein expression between lesional PsA and PsC skin.
In order to further characterise these in vitro cellular responses we incubated PBMCs with and without an optimal concentration of the MAb (100-300 micrograms ml-1), as defined by the proliferation assay, and compared the differences in cell subpopulations.
Thus, differences in the outcome of these assays must reflect the differences in CD4+ T cells, which also are the only cells capable of proliferation.
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