Exact(14)
Gels were scanned using an Image Scanner UMAX, Amersham (300 dpi, 12-bit image), which allowed us to obtain spot intensities in pixel units.
Results were visualized by Chemilumi-One (Nacalai Tesque) and captured using an image scanner.
Stained gels were scanned using an image scanner, and images were processed using ImageMaster2D Elite (version 3.01) software.
For densitometric quantification, the films were scanned using an Image Scanner (Amersham Pharmacia) and analyzed using ImageMaster.
Images of 2D gels are acquired into a database using an image scanner.
Images were acquired using an Image Scanner Model UTA-1100 (Amersham Biosciences).
Similar(46)
Proteins were stained with the GelCode reagent (Pierce, Rockford IL, USA), and the gels scanned using an Amersham Image Scanner digitalizer prior to computer processing.
After electrophoresis, the gel was scanned using a Typhoon image scanner and the images were analyzed using the DeCyder software.
Gels were then scanned for fluorescence with λex/λem 635/670 nm for Cy5-NHS and 532/580 nm for Cy3-NHS using a fluorescence image scanner FLA-70000, Fujifilm Life Science) and silver-stained as described previously [28].
The film plates were scanned using a Zeiss Imaging scanner (Z/I Imaging Corporation) with a step size of 14 μm, resulting in a pixel size of 2.82 Å.
Radiographic images were scanned and digitalized using an electronic scanner, and JPEG image compression was used to facilitate the transmission of radiographic images and patient charts.
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