Your English writing platform
Discover LudwigSuggestions(2)
Exact(13)
As we suspected, the average values obtained for fl-OPN levels were highly variable between assays using the same group of breast cancer patient samples (Fig. 4).
It is relevant to mention that the recombinant protein TvLEGU-1r obtained in this study did not have proteolytic activity and could not be activated (data not shown) for biochemical and direct functional assays, using the same reported conditions [ 58].
This result was confirmed by quantitative RT PCR assays using the same primers in exons 1 and 4. The reduced level of the exon 1−4 splice form can be explained by the strong transcription terminator present at the 3′ end of the promoter-trap sequence (Friedrich and Soriano 1991).
The three samples were selected according to the availability of (i) plasma Aß concentration assays using the same method (the INNO-BIA plasma Aß forms assay; this point is of particular importance, since the assay methodology can significantly influence interpretation of the data [16]), (ii) SBP and DBP measurements; (iii) information on demographic variables, smoking and medication use.
To examine the effects of bufalin on cell migration, we performed wound healing and transwell-migration assays using the same two hepatoma cell lines.
To test this hypothesis, we performed a prospectively designed comparison between these assays using the same formalin-fixed, paraffin-embedded (FFPE) tumor samples.
Similar(47)
FLPe assays used the same conditions as Cre assays except that the annealing temperature was raised to 70°C.
Such differences would be unlikely, because all commercially available anti-CCP assays use the same antigen strips [ 20] and differ only in technical aspects of the ELISA itself.
For example, such intuitive knowledge would have predicted small differences in performance between Assay 1 and Assay 2 because both assays used the same primers at the same A&E temperature.
The reaction mixtures assayed using the same procedure in the absence of MamK proteins served as negative controls.
In this study, the newly developed triplex real-time PCR assay was compared with a quadruplex conventional gel-based PCR assay using the same primer sets in both assays.
Write better and faster with AI suggestions while staying true to your unique style.
Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com