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Thus we only need to check that the assumptions (i), (ii) of Lemma 3.4 are valid for our functional I.
For our functional tests and experimental evaluations, we used the indoor mesocosm facility at Umeå Marine Sciences Centre, University of Umeå, Sweden, situated at the northern Bothnian Sea (N63°34′; E19°50′) in the Baltic Sea.
For our functional studies on p24, we generated Xenopus laevis transgenic for the p24α3 or the p24δ2 protein.
For our functional analyses, we further restricted our data to only use well-curated genes across different yeast genomes (see Methods).
The spatial co-ordinates of these ROIs were re-sampled to match the FOV and voxel size used for our functional analyses.
For our functional studies, we focused on the pheromone components (Z,E -9,11-tetradecadienyl acetate (Z,E -9,11-tetradecadienyl12-tetradecadienyl acetate (Z,E -9,11-tetradecadienylt volacetateZ)-3-hexenyl Z9E11-14 Ac-6:and.
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Here, we get our results concerning the n-exponential convexity and exponential convexity for our functionals (Lambda_{k}), (kin{1,2}), as defined in (A1) and (A2).
A further justification for narrowing our functional analyses to NF90 is that NF90 alone showed a partial relocalization to the cytoplasm of dengue virus-infected cells (Figure 4), and we hypothesized that the relocalization may have regulatory significance for dengue virus RNA translation or replication.
We use soft substrates with physiologically relevant elastic modulus for all our functional assays, but fibroblasts may behave differently on rigid substrates.
In the first optimization step using Ex4-yeasts as a model for our novel functional assay system, we remarkably found that DMEM buffered at neutral pH designed for mammalian cell culture was very suitable for yeast peptide secretion and GLP1R activation in mammalian cells, even though yeast cells could not grow in the medium.
However, this 3 nt periodicity was not observed on average for our predicted functional regions, demonstrating that they are generally not exonic.
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