Sentence examples for strain cells from inspiring English sources

Specific reasons for failing to detect mixed infections would include low initial numbers of minority strain cells in sputum, stochastic growth in culture and the physical division of initial samples into parts (typically only one of which is genotyped).

To verify this hypothesis and to test whether short-term adaptation helps to retain tolerance in the evolved strain, cells from the biofilm, CC156 and TMB3500 were inoculated in liquid media with inhibitor concentrations similar to the residual inhibitor concentrations in the liquid suspension of the ALE chemostat.

Wild-type strain and mutant strain cells were grown as described above and harvested for RNA extraction.

For each bacterial strain, cells were recovered from 4 different leaves; two samples were collected from each specimen leaf.

Yeast plasmid DNA was extracted from clones that grew on QDO medium, electroporated into Escherichia coli KC8 strain cells, and the bacterial plasmids isolated and sequenced.

In experiments using the cim3-1 strain, cells were preincubated for 1 hour at 37°C prior to the addition of cycloheximide.

To ensure that the intrinsic differentiation profiles of NPCs from each mouse strain cells were similar, neurospheres were dissociated and cultured under differentiating conditions that promote the accumulation of both neurons and glia [49].

In the second stage of OPEN selection, selection strain cells were again grown in 24-well blocks but in 1 ml of NM medium supplemented with 30 μg/ml chloramphenicol, 30 μg/ml kanamycin, and no IPTG.

To construct an auxin-inducible degron-Tub4 (TUB4-AID) strain, cells of YPH499 [57] were transformed with an integration plasmid encoding the F-box transport inhibitor response 1 (TIR1) gene driven by the ADH1 promoter.

For transformation, 300 ng of each plasmid expressing ArntbHLH-C/EBP, ArntbHLH, or Arnt-C/EBP were electroporated with 40 µL competent reporter-strain cells using a preset program for S. cerevisiae (Voltage: 1500 V, Capacitance: 25 µF, Resistance: 200 Ω, 2 mm gap cuvette).

The influence of antigen location, inside or on the surface of carrier-strain cells, on the efficacy of vaccination has been tested multiple times.