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This expression analysis confirmed that DLD1Tr21/NBPF1 and DLD1Tr21/Mock cells expressed EGFP upon dox addition (Fig. 13A), and that NBPF1 expression was induced only in the DLD1Tr21/NBPF1 cell line in the presence of dox (Fig. 13B).
Expression analysis confirmed that some of these genes were specifically expressed in fetal ovaries.
Furthermore, protein expression analysis confirmed that proteins involved in cardiac differentiation and functionality were highly expressed in the treated cells.
Our expression analysis confirmed that this Nfatc2 transcript, named here Nfatc2IB-IIS-VIIa, is expressed in the mouse brain.
There were many putative light responsive elements in all the seven promoters of genes, and the expression analysis confirmed that the seven genes were induced by light.
Quantitative expression analysis confirmed that Oct-4 expression declines during differentiation, as in wildtype ES cells (Figure S3D).
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We validated miR-29b regulatory activity by luciferase reporter assay as well as by Sp1 mRNA and protein expression analysis, confirming that miR-29b is able to downregulate Sp1.
Differential host gene expression analysis confirms that the presence of Moraxella catarrhalis is associated to a specific M. catarrhalis core gene signature expressed by the host.
Our results from the expression analysis confirm that the aleurone color difference between Pr1 and pr1 is due to the lack of Zmf3′h1 transcripts in pr1 and not due to any absence or change in the expression of other anthocyanin biosynthetic or regulatory genes.
Our expression analysis confirmed the NRSE screen and showed that the expression of four putative F-box genes is localized to neural tissues during Xenopus development.
RT-PCR analysis confirms that Ntl expression is male-specific and limited to the testes (Fig3A).
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com