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Every move he made was examined under a microscope until the parties reached a breaking point.
Nematode development was monitored daily under a microscope until the formation of infective juveniles.
To differential passage, satellite cells were treated to a mild trypsinization and observed under a microscope until the round satellite cells were seen detaching from the plate.
Urine flow was observed under a stereoscopic microscope until the fluorescence reached the urinary bladder, or until the time following administration exceeded 30 min. The cilia of the hatchlings were subjected to length measurement.
Leaf discs were observed under the microscope until the first mating occurred, which happened within 5 minutes in all replicates.
Images were captured under 40× magnifications every 8 12 hours using a phase-contrast microscope until the completed closure of the wound was observed in the vehicle-treated control.
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The oncospheres were checked every 2 min with a microscope until all the oncospheres had been released from embryonic membranes.
Protoplast formation was monitored using a microscope until ≥99% of the cells was lysed when SDS was added (1% SDS w/v).
It notably showed that the double layer capacity was directly proportional to the active surface measured by the microscope observation until the surface was totally covered, according to the expectations in the experimental conditions used here.
We chose the sampling area for background silver grains by moving the microscope stage until the tissue was no longer visible.
For pHmito/Ψ m recordings, cells were incubated at room temperature for 20 min with 4 nM TMRM, washed, and kept at 37°C on the microscope until signal reached stability.
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