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Conclusions: The ability for QLF to detect and longitudinally monitor in vitro erosion has been shown.
New knowledge about mechanisms involved in biofilm formation have recently been obtained by the use of optical tools to monitor in vitro grown biofilms.
To monitor in vitro development, transgenic and nontransgenic SCNT embryos were cultured for 6 days until they reached the blastocyst stage.
When impedance measurements reached maximal values (cocultures reached TEER values of 890.9±17.9 OGD×cm2), OGD was induced to monitor in vitro ischemia-induced BBB breakdown.
Currently, one of the standard ways to assess drug efficacy against liver stages is to monitor in vitro liver stage development by quantitative RT-PCR (qRT-PCR) methods [21] [23] [24], [25] that are time consuming and expensive.
These assays were used to monitor in vitro activation of plasma FSAP by cells.
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We have used potassium permanganate (KMnO4) probing assay to monitor in-vitro opening of the DNA helix.
In order to test these experimentally, tissue samples were monitored in-vitro during treatment at multiple wavelengths.
The release kinetics of SIM was monitored in vitro spectroscopically.
In this study, cell surface GSLs were monitored in vitro at five different time points: undifferentiated (Day 5), confluent (Day 7), partially differentiated (Day 14), differentiated (Day 21), and post-differentiated (Day 24).
To achieve this, we exploited the l-glutamate dehydrogenase coupled assay that has previously been shown to allow for aminotransferase activity to be monitored in vitro.
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