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Displacement was monitored using an optical sensor with submicrometer sensitivity.
Extracellular zinc was monitored using 50 μM FluoZin-3.
Intracellular calcium was monitored using 1 μM Fluo-4-AM and extracellular zinc was monitored using 50 μM FluoZin-3.
Improvement was monitored using standardized instruments.
The modification process was monitored using electrochemistry, SEM, XPS.
ROS generation was monitored using 2,7-dichlorofluorescin fluorescence.
The damage accumulation was monitored using Rutherford backscattering spectrometry (RBS).
Surface crack growth was monitored using Image Processing Technique (IPT).
Throughout the refinement, the geometry of the structure was monitored using the program Molprobity53.
The organelle specific probe fluorescence was monitored using the settings recommended by the manufacturer.
Ethanol consumption was monitored using two different DID protocols (Rhodes et al, 2005).
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