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After 5 days, thymidine was added (0.4 μCi per well; Amersham Pharmacia Biotech, Buckinghamshire, UK) for 16 h, after which the cells were harvested onto fiberglass filters and H-thymidine incorporation was determined using a flatbed scintillation counter (Wallac, Turku, Finland).
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In the year 2000 we scanned from them using a flatbed scanner with transmitted light.
Results were obtained using a flatbed scanner and analysis by the self-written program optimized to manual reads.
The signals generated after gold deposition and silver enhancement, were quantified using a flatbed scanner having 2-μm resolution.
Microarrays were scanned at 2400 dpi using a flatbed scanner (Cannon, Søborg, Denmark) and converted to grayscale TIFFs.
The nodal roots were scanned using a flatbed scanner at a resolution of 600 dpi (HP ScanJet II, Hewlett Packard, USA).
The autoradiographic images were digitized using a flatbed scanner.
Films were scanned into Photoshop (Adobe) using a flatbed scanner and adjusted for brightness and contrast.
Gels were imaged using a flatbed scanner.
Incubated blot strips were digitalized using a flatbed scanner.
Samples were subjected to SDS-PAGE and visualized in-gel using a flatbed fluorescence scanner (MiraBio).
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