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RNA interference was monitored by analysing EWS FLI1 protein and mRNA levels using western blot and qRT PCR, respectively.
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In standard mode, m/ z 75 for As and m/ z 77 for ArCl interference were monitored.
The potential for peptide interferences was monitored with AuDIT software [ 48] and signals marked as problematic were removed.
Ar-scattered interferences were monitored at half masses for elevated background correction.
The interference-free isotope Se was monitored.
The release of AF 6 was monitored at interference free potential region (–50 mV vs. Ag|AgCl) using differential pulse voltammetry as signal read-out.
The distribution of TssK was monitored by interference optics at 3-h intervals at a rotor speed of 9000 rev./min until the system had reached equilibrium.
Excimer fluorescence was monitored using a 475 nm interference filter.
The potential formation of carbon-containing cluster ions was monitored by measuring blank planchets, but no interferences were detected.
The target made of point diffraction sources emanates two spherical wavefronts, of which interference intensity is monitored by the photo-detectors.
In addition, the interference level should be monitored for handover decision.
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