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Cerl-GFP-expressing cell shape was monitored over the course of 2 h of live imaging in freshly collected 'in vivo' embryos (c) and in vitro-cultured embryos.
The spike waveform shape was monitored during recording to ensure good spike isolation (Fig. S1).
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Moreover, the GNPs size and shape are monitored by the transmission electron microscopy (TEM).
The cell shapes were monitored after 96 h of transfection and images were captured using an Olympus IX70 microscope equipped with digital camera (Olympus, Inc., Melville, NY, USA).
The micropipette was carefully inserted through the hollow screw into the microfluidic chamber while the tip of the pipette entering the intersection-zone within the T-shape microfluidic channel was monitored visually.
The shape of the flames was monitored by taking OH* images with an EM-CCD camera.
(B) C. difficile R20291 pJS116, KNM6 pJS116 and KNM6 pKM142 were grown in TYG (closed shapes, ●) or TY (open shapes, ○) medium and growth was monitored over time.
The shape of the galactosylated polylysine complexes was monitored by circular dichroism and electron microscopy (Philips EM 400, Fei Company Electron Optics, Eindhoven, Netherlands).
Immediately following response shaping on each lever, the animal was monitored to make sure the response was learned, and then left in the chamber for an additional 15 min to further strengthen the newly learned behavior.
This zone shape as well as its evolution during crack growth was monitored.
A second group was monitored, and given a $1 reward for each shape that was successfully replicated.
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