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Therefore, in this first assay, synchronized adults were fed with Paraquat (1,1′-dimethyl-4,4′-bipyridylium 1,1′-dimethyl-4,4′-bipyridylium 1,1′-dimethyl-4,4′-bipyridylium 1,1′-dimethyl-4,4′-bipyridylium cells andichloriderenewandindependent of the late response involving increased ISC proliferation.
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In this second assay, there was again no significant difference in the onset times that depended on the presence of ATP (Fig. 2B, first bar).
Using this second assay, we clearly show that Pten−/− differentiated teratoma-initiating ECCs have 5 times greater colony forming potential than wild type cells, suggesting increased capacity for ECC survival and self renewal over wild type (Fig. 4B).
Following WHO criteria, this third assay determined the final result.
Thus, this second assay looks only at the direct effect of high levels of LPS interacting with histones, causing the histones to release from the droplets.
We developed this second assay because the school comprises the only form of shelter in the tank in the model school assay, so fish could follow the school as a result of an increased tendency to school or as a consequence of shelter-seeking behavior.
This is the first assay to allow the quantitation of NQO1 in live cells which can then be retained for further experiments.
To our knowledge, this is the first assay designed for the simultaneous detection and genotyping of WNV by rapid, sensitive real-time PCR which may be implemented in diagnostic and epidemiology laboratories.
To our knowledge, this is the first assay that is capable of evaluating complement activation mediated by Ficolin-3 and down stream components and thus will provide a critical supplement to the already existing assays for evaluating complement function and genetic defects.
This is the first assay system for studying a TP retrotransposon in a simple microbial model system and it should significantly advance the study of these elements.
Moreover to the best of our knowledge, this is the first assay reported so far that provides additionally a semi-quantitative estimation of CST6 promoter methylation.
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