These gels were stained with Coomassie blue and scanned for documentation after SDS-PAGE.
The film was photographed and scanned for documentation.
Gels were stained by ethidium bromide, visualized, and then scanned for documentation.
After electrophoresis, the gels were incubated overnight at 37°C in 0.1% Triton X-100, 5 mM CaCl2, 1 mM ZnCl2, 3 mM NaN3, and 50 mM Tris pH 7.4 in a closed container, and then stained with coomassie blue, and finally destained, dried, and scanned for documentation.
Final electrophoresis was done at 20 mA constant current using 5.1% acetic acid as running buffer for 1 h at RT. Gel was stained with 0.125% coomassie blue (in 40% methanol, 7% glacial acetic acid and 53% DW) for 10 min at RT. Gels were destained in a solution of 40% methanol, 7% glacial acetic acid, 53% DW at RT. Coomassie stained protein bands were scanned for documentation.
Their therapy, however, was with tubes that were not radiologically guided and with no CT scan documentation of the effect of therapy.
The blots were developed using chemiluminescent solution (Immobilon Western, Millipore) and scanned by gel documentation system (LAS 3000, Fuji, Shizuoka, Japan).
In addition, the websites of the municipalities and agencies were scanned for further documentation on safety policies and ongoing programmes.
The gels were subjected to Coomassie brilliant blue (CBB) stain for 4 h, followed by destaining and scanned by gel documentation system (Syngene, Frederick, MD, USA).
Gels were scanned on a Gel documentation system (GelDoc-XR, Bio-Rad, Hercules, CA, USA).
The gel was scanned using the gel documentation system, AlphaImager HP, Cell Biosciences (Santa Clara, CA).
