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The total proteins include the control and those treated with Fe3O4 nanoparticle, and the marker is demonstrated in Figure 5.
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The utility of asRNAMqsA as a counterselection marker was demonstrated by efficient plasmid curing and strain improvement experiments.
Finally, the utility of DBP as diagnostic marker was demonstrated on individual sera from 20 bovine TB infected and 10 control animals with 95% sensitivity and 90% specificity.
The utility of amine-reactive tag 1 as a 2PA biological marker was demonstrated by incubation with HeLa cells.
We included studies in which a selected marker was demonstrated to have a prognostic value alone or in combination with other markers (not strictly connected with inflammation).
The potential utility of this molecular marker was demonstrated when it was applied to a set of unrelated germplasm that was also varying for presence/absence of γ-D.
Only the residual expression of the marker was demonstrated in adjacent tubules showing arrest of spermatogenesis at the level of spermatogonia or primary spermatocytes, as well as normal spermatogenesis.
Specificity of the staining for different cell markers (except for the endothelial marker) was demonstrated using an irrelevant, isotype matched mAb 1C11, 3H12 and 13D12 [ 34] and by the deletion of primary antibodies (pAb anti-human VWF and anti-PCV1 pAb), and by the complete absence of PCV1-specific fluorescence in tissue sections of non-inoculated, age-matched foetuses.
The capability of the sensors to detect even single markers is demonstrated by a model experiment.
The co-dominant nature of microsatellite markers was demonstrated by pedigree and by segregation analysis.
In addition, 11 out of 12 markers were demonstrated to be highly transferrable to other closely related species.
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