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Phosphorylation in the PI3K-AKT-mTOR signaling pathway: Western blot analysis was applied to examine PI3K-AKT-mTOR pathway components potentially involved in P2X7R-enhanced PDLSC osteogenesis.
Upstream signals involved in the potential pathway: Western blot analysis (see Section Western blot analysis) was applied to evaluate protein expression profiles in PDLSCs (with Ad-P2X7R transfection or Ad-control transfection) in response to inflammation and/or addition of P2X7R agonist/antagonist.
To obtain quantitative data of these specific sites, the ligation-mediated polymerase chain reaction technique, instead of Southern blot analysis, was applied.
Western blot analysis was applied to observe the expression of osteogenic-related proteins after treatment with different concentrations of earthworm extract for 7 days.
Real-time PCR was used to quantify the expression of Axin, and western blot analysis was applied to measure protein levels of Axin, β-catenin, Cyclin D1, MMP-7, DNMTS, MeCP2 and acetylated histones.
Western blot analysis was applied to two identified markers to validate the expression of intact proteins by an antibody-based approach and observed by mass spectrometric analysis using expression of digested peptides.
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Quantitative real-time PCR (qPCR) and western blot analysis were applied to validate gene expression profiling.
SDS-PAGE and Western blot analysis were applied to analyze the purity and to identify the recombinant swollenin.
The subtraction suppression hybridization (SSH) technique and northern blotting analysis was applied to explore the pluripotency-associated genes under a unique epigenetic sub-microenvironment.
Densitometry analysis was applied to each blot to quantify the intensity of bands, followed by normalization against loading controls.
Thematic analysis was applied.
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