Sentence examples for medium was grown from inspiring English sources

Preculture in reactivation medium was grown aerobically at 30°C with reciprocal shaking at 150 rpm.

Standing cultures containing 3 ml of M63 medium were grown for 6 days at 25°C in 12-ml polystyrene culture tubes (17×100 mm, Greiner Bio-one).

E. coli cultures in TB medium were grown at 37°C to an optical density (600 nm) of 1.5, induced with 1 mM isopropyl-β-D-thiogalactoside, and allowed to grow for an additional 6 hrs at 20°C.

As for different temperature conditions, overnight log phase cultures of WP3 cells diluted 1000-fold by the same medium were grown at 4°C or 25°C for 3 days to reach an equivalent optical density.

Plantlets recovered after growth on regeneration medium were grown on MS medium without hormones and without bialaphos.

Seedling cultures in liquid medium were grown in ½ Gamborg medium (Duchefa, Harlem, The Netherlands) with or without 0.5% sucrose and the medium was exchanged after 7 days.

BAC clones of HindIII 96-deep-well blocks containing 1.2 ml/well of 2xYT medium were grown overnight at 37°C with shaking at 300 rpm.

MDA-MB-231-ShNC (cultured in light medium) and MDA-MB-231-ShB Cells (cultured in heavy medium) were grown in doublet SILAC conditions and the proteomic samples were prepared as previously described [ 16].

E1A.NR3 retinal cells at a density of 104 cells/well in 200 μl DMEM medium were grown with purified serum IgG from patients and controls, at 150 μg/ml for 48 hrs.

Control cells without chemical stressor in the added 25 mL of M9 medium were grown for approximately 0.5 h to reach the same OD600, 0.6-0.7, as the chemically stressed conditions.

MiPS (2 × 10 cells/10 ml medium) were grown in suspension for 3 days in high glucose DMEM containing 10 % FBS, 0.5%% penicillin/streptomycin, 0.1 mmol/L non-essential amino acids, and 0.1 mmol/L mercaptoethanol) [ 2].