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The in vitro effect of corticosteroids on the protein expression of peripheral blood granulocytes will be assessed using fluorescence 2-dimensional difference (2D) gel electrophoresis [ 38].
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48 h after the first infection, the expression of green fluorescent protein was assessed using fluorescence microscopy.
The alteration of RBC membrane was assessed using fluorescence anisotropy (FAn) and fluorescence probes with different affinities for varying sections of the membrane phospholipid bilayer.
Smears were assessed using fluorescence microscopy and culture using Lowenstein-Jensen media.
Transduction efficiency was assessed using fluorescence microscopy and flow cytometry.
Diffusion of alginate in mucus was assessed using fluorescence recovery after photo-bleaching (FRAP).
HER2 and EGFR gene amplification were assessed using fluorescence in situ hybridisation.
The replication time of specific loci were assessed using fluorescence microscopy (Kitamura et al., 2006; Saner et al., 2013).
Relative cell attachment on the laminin coated wells were assessed using fluorescence plate reader at an excitation wavelength of ~485 nm and an emission wavelength of ~520 nm.
To check whether CENH3-GFP allows for the detection of colchicine-induced endomitotic polyploidy, nuclei in these newly formed organs were assessed using fluorescence microscopy.
Amplification of 11q13 was assessed using fluorescence in situ hybridisation (FISH) probes for FGF3/INT2, FGF4/HST1 or CCND1 (Lese et al, 1995; Shuster et al, 2000).
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