Sentence examples for both constructs were grown from inspiring English sources

Strains containing both constructs were grown to competence and analyzed by fluorescence microscopy.

The structures expressing individual shRNA constructs were grown for 15 days to reach quiescence.

Cell/scaffold constructs were grown in vitro for 7, 14, and 28 days.

Constructs were grown in static culture for 12 days and then decellularized by rapid freeze thaw cycling.

Control constructs were grown in parallel, and all groups were evaluated for gross morphology, histology, cellularity, collagen and sulfated glycosaminoglycan (GAG) content, and compressive and tensile mechanical properties.

For the in vivo investigation of protein localization, EBY.VW4000 cells expressing the indicated constructs were grown in selective SCM-Ura media without Methionine until an OD600nm = 2.0 2.5 was reached.

Self-assembled constructs were grown for 4 weeks using a previously established method and were subjected to continuous 7-day treatment with 30 mM ribose during culture weeks 1, 2, 3, or 4, or for the entire 4-week culture.

In Phase I self-assembled constructs were grown for 4 weeks and subjected to treatment with the TRPV4 agonist 4α-phorbol-12,13-didecanoate (4α-PDD) during three treatment time windows: t = 6 10, t = 10 14, and t = 14 18 days.

Left, yeast cells carrying different constructs were grown for 2 d at 30°C in SD-Leu-Trp agar medium.

Agrobacterium cells containing split YFP fusion constructs were grown in liquid yeast extract peptone (YEP) medium supplemented with antibiotics (spectinomycin 50 μg/ml and Rifampicin 50 μg/ml).

Constructs were grown in PD98059 supplemented medium for the given time points.