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In normal room light, it was hard to distinguish the electronic type from its background.
The measurements were performed under normal room light at 25°C.
Colonies of GFP-labeled and parental strains had identical morphological characteristics on TSA plates, except that some GFP-labeled colonies appeared light green or yellow when observed visually under normal room light.
The dissection was performed in normal room light using light-adapted frogs.
On the day of an experiment, rats were dark-adapted overnight and half were subjected to normal room light (~300 lux) for 30 min.
Individual dehydrated samples were then placed into 50 mL tubes and hydrated overnight in 40 mL of deionized water to full turgidity under normal room light and temperature.
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The welding was done in air, at room temperature, under normal room lighting conditions.
Sibling embryos that were not subjected to light aside from normal room lighting were reared in the same medium and on the same microscope stage to ensure the same temperature as the imaged embryo.
To confirm the coincidence between the timing of the MBT and the time at which cell cycles arrest in response to HU treatment, we measured the abundance of pY15-Cdc2 in embryos that were only exposed to normal room lighting in the presence or absence of HU (Figure 4E).
The intervention was a randomised 8-week trial with three groups: aerobics in bright light, aerobics in normal room lighting, and relaxation/stretching in bright light.
The drugs were studied at their highest commonly infused concentrations and exposed to three variations in environmental conditions (diluent: sodium chloride 0.9% or glucose 10%; temperature 25 or 37°C; and normal room lighting or blue light phototherapy).
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