Sentence examples for media containing normal from inspiring English sources

HFFs were grown in either 'light' media containing normal lysine and leucine, or 'heavy' media containing N15/C13-labeled N15/C13-labeledine.

These studies were performed with distal tubule epithelial cells, MDCT, cultured in media containing normal (1.0 mM) or low (nominally magnesium-free) magnesium concentrations for 16 h and on kidney cortex tissue harvested from mice maintained on either normal or magnesium-restricted diets for 5 days.

Myofibroblasts incubated for 1 h in Ca2+-free media phosphorylated significantly less Smad2/3 in the presence of TGFβ1 (10 ng/ml) than those incubated in media containing normal external Ca2+, P = 0.0439 (one-way ANOVA, corrected by Sidaks multiple comparison test).

To model in situ hydrogel formation, hydrogel mechanical behavior was characterized using rheological testing following incubation in media containing either normal (1.8 mM) or elevated (6 mM) Ca2+ concentrations.

Rheological analysis demonstrated that all hydrogels tested within this study exhibit an increase in magnitude of the LVE limit after being incubated in media containing either normal (1.8 mM) or elevated (6 mM) levels of Ca2+ for a period of either two or five days at a temperature of 37 °C.

Cells were incubated for an additional 24 hours in media containing 5 mM (normal) and 25 mM (high) glucose.

Time tests were performed to determine the ultimate elastic modulus (UEM) of hydrogel blends after incubation in media containing either low (normal) or high (elevated) concentrations of Ca2+.

MCF-7 cells were grown in phenol free EMEM/CD-FBS media for 4 days prior to drug treatments and MCF-7/shRNA ERRα RNAi cells were maintained in normal media containing whole serum (described above).

MCF-7 cells were maintained in phenol free EMEM/CD-FBS media for 4 days prior to drug treatments (in triplicate) and MCF-7/shRNA ERRα RNAi cells were maintained in normal media containing whole serum (described above).

Next day the cell monolayer was exposed to fresh low serum medium of different treatment conditions containing 5.5 mM (normal/control), 35.0 mM d-glucose (HG), normal media containing 5% CSE, HG media containing 5% CSE.

The cells were cultured as detailed above and were treated for 24 h with 35.0 mM d-glucose (HG), normal media containing 5% CSE, HG media containing 5% CSE, apart from 5.5 mM (normal/control) exposure.