Sentence examples for biosensor was monitored using from inspiring English sources
In the measurement of E. coli DH5 (as a model target), the change in interfacial electron transfer resistance of lectin-based biosensor was monitored using a redox couple of Fe CN 63−/4−.
To evaluate the role of Rac1 GTPase in mechanical regulation of MMP13, Rac1 activity of C28/I2 chondrocyte cells was monitored using the Rac1 biosensor and FRET imaging.
Western blot analysis was performed to determine the phosphorylation levels of p38 MAPK and NFκB, and activity of Rac1 GTPase was monitored using a fluorescence resonance energy transfer (FRET) technique with a biosensor specific to Rac1 GTPase.
Cellular internalization of biosensor was monitored by confocal laser scanning microscopy and quantified by flow cytometry.
Steady-state equilibrium binding of conformation dependent human H5N1 neutralizing MAb FLA5.10 was monitored at 25°C using a ProteOn surface plasmon resonance biosensor (XPR36, BioRad Labs).
In continuous assays, phosphate release was monitored in real time to quantify kinetic parameters using the fluorescent phosphate biosensor N- 2-[1-maleimidyl]ethyl -7- diethylamino coumarin-3-carboxamide N- 2-[1-maleimidyl]ethyl -7- diethylamino coumarin-3-carboxamide N- 2-[1-maleimidyl]ethyl -7- diethylamino coumarin-3-carboxamide N- 2-[1-maleimidyl]ethyl -7- diethylamino coumarin-3-carboxamide N- 2-[1-maleimidyl]ethyl -7- diethylamino coumarin-3-carboxamide N- 2-[1-maleimidyl]ethyl -7- diethylamino coumarin-3-carboxamide N- 2-[1-maleimidyl]ethyl -7- diethylamino coumarin-3-carboxamide N- 2-[1-maleimidyl]ethyl -7- diethylamino coumarin-3-carboxamide
The Corning Epic® optical biosensor was used to monitor dynamic mass rearrangements within and proximal to the cell membrane in tumor cell lines derived from cancers of the colon, bone, cervix, lung and breast.
In SPR biosensor applications, light is monitored and analyzed to extract binding and kinetic information.
Assimilation of orthophosphate by microorganisms has been monitored by the use of FRET biosensors on Synechococcus strains by engineering the genes encoding for the phosphate-binding protein [41].
Kinetics of phosphorylation of d--glucose by hexokinase from S. cerevisiae (Sigma-Aldrich) were monitored with the ADP biosensor 5-ATR-ParM (His6/K33A/D63C/T174A/T175N/D224C/C287A) using a Cary Eclipse spectrofluorimeter (Varian).
