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Effects of compounds were analyzed by measuring the area covered by migrating cells using Image-Pro Analyzer software to track the migration front.
The electrochemical characteristics of MFMEC and its relation with decolorization were analyzed by measuring cathode potential, EIS and current change.
Kinetic parameters were analyzed by measuring enzyme activities against guaiacol, DMP and ABTS (as described above) over the concentration range 5 95 µM under the optimal assay conditions.
Finally, the potential histopathological changes were analyzed by measuring the accumulations of glycosaminoglycans and hyaluronic acid, the expressions of CD44 and TLR2, and DNA fragmentation in the cochlea.
Main Outcome Measures: Kinematics of head and hip were analyzed by measuring periodic shift of LED markers using an optoelectronic device.
Proteolytic activity of both calpain system and key enzymes of the UPP were analyzed by measuring protein levels of calpain1, calpain2, and the muscle-specific E3 ligases MAFbx and MuRF1 [7, 17].
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Biomass accumulation was analyzed by measuring OD660 of the culture after every 24 h.
The photocatalytic efficiency was analyzed by measuring absorption spectra of the degraded MB solution.
Proliferation of T cells was analyzed by measuring the incorporation of [3H]-thymidine.
The growth was analyzed by measuring optical density at 660 nm (Heliose Spectrophotometer, Thermo Spectronic, USA).
Moisture of samples was analyzed by measuring loss of weight at 70 °C.
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