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In this article we evaluated the concept of bacterial cell count monitoring using flow cytometry as a tool to determine antimicrobial susceptibility in antibiotic broth-dilution series.
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The intracellular uptake was measured and monitored using flow cytometry and fluorescence microscopy, respectively (Figure 3).
The viability of bacteria during biotransformation reactions was monitored using flow cytometry.
Cerebral blood flow, as well as blood pressure and heart rate were monitored using flow probes in Beagle dogs.
Fluorescence intensity was monitored using flow cytometer (Guava Technologies, Hayward, California, USA).
The presentation of total antigens was monitored using flow cytometry.
The cells containing fluorescent polymers were monitored using flow cytometry.
The adipocytic differentiation was monitored using flow cytometry with different markers - see also Methods.
The fluorescence of the cells was monitored using flow cytometry (FACSCalibur, BD, Franklin Lakes, New Jersey, USA).
Once washed and re-suspended in PBS, the loss of red fluorescence was monitored using flow cytometry.
Loss of DiOC6 fluorescence indicates reduction in the mitochondrial inner transmembrane potential, which was monitored using flow cytometer as described before.
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