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The sections were examined by UV light microscopy and EGFP positive cells were counted (Figure 4B).
All samples were examined by UV light microscopy.
The UV light microscopy test allowed us to appreciate a definitive status.
Cytospins were prepared, mounted in fluorescent mounting medium (DAKO, Glostrup, Denmark) and viewed by UV light microscopy (Nikon, Melville, USA).
Fluorescein isothiocyanate (FITC -conjugated phalloidin (Sigma) was used to evaluate cytoskeleton actin distribution on tubular cells and podocytes by ultraviolet (UV) light microscopy.
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GFP can be detected easily by fluorescence colony counting under long wavelength UV light, epifluorescence microscopy, laser confocal microscopy, and flow cytometry for individual cells or direct fluorescence measurement.
The accumulation of GFP was followed and imaged with a hand-held UV light and fluorescence microscopy for 3-7 days post-inoculation.
TMV.GFP infection was monitored by examination of inoculated leaves under UV light, by confocal scanning laser microscopy and by epifluorescence microscopy.
Accumulation of both stilbenes and pathogen mycelia was detected in foliar tissues by epifluorescence microscopy (under UV light).
References of PUR slabstock foams (ether-based polyols and toluene diisocyanates) were produced; and infrared micro-spectroscopy and optical microscopy (under darkfield, polarised light and UV light) were selected to assess PUR ageing.
A key element related to microscopy is the use of a transmitted UV light source rather than incident (epifluorescence) light.
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