In order to determine if mTORC2 is activated in ΔF508 cell41o- celysatestes, we measured expression of mTOR and phosphorylation of the mTOR protein at serine 2481.
We estimated the TF activities based on the qPCR measured expression data from bmp8b TG vs. WT mice using the "msviper" method from the "viper" R package (https://doi.org/10.1038/ng.3593).3593
To assess radiation-induced response of protein markers in human lymphocytes irradiated ex vivo, we measured expression levels of our three best candidates, FDXR, DDB2 and ACTN1 protein, 3 days after initial exposure (Fig. 4B).
We measured expression and used biochemical characterization of multiple carbohydrate esterases by the xylanolytic rumen bacterium Prevotella ruminicola 23 grown on an ester-enriched substrate to gain insight into the carbohydrate esterase activities of this hemicellulolytic rumen bacterium.
We also measured expression levels of classical HLA genes in eight HLA homozygous reference cell lines at baseline and after three treatments (heat shock, LPS, and IFN-gamma).
Using the Enterococcus faecalis alkaline phosphatase gene, phoZ, we measured expression of C. difficile genes using a colorimetric alkaline phosphatase assay.
We measured expression and production of myoblast markers: paired box-7 (Pax7), myogenic differentiation factor-1 (MyoD), myogenin (MyoG), myogenic factor-6 (Myf6), and myosin heavy chain (MyHC).
The researchers measured expression patterns of four genes active in the enamel knots.
To study the roles CD44 molecules play in inflammatory synovitis, we measured expression of CD44 in inflamed and noninflamed synovial fluid and tissue, using indirect immunofluorescence assays on tissue sections and quantitative Western blot analysis.
Measured expression levels are all relative to these references.
Using the re-array, we measured expression in triplicate for 10 different rice organs (Figure 2A and S4).
