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The transformation of gDNA could be visualized by detection of fluorescence resulting from the expression of fluorescent proteins.
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Reaction products were visualized by detection of chemiluminescence using an ECL kit (Amersham Biosciences, Piscataway, NJ, USA).
CSP on the surface of sporozoites was visualized by detection with mAb 3D11 specific for the CSP repeat region or polyclonal rabbit N-terminal CSP serum.
Replication foci or 'factories' can be visualized by immuno-detection of replication enzymes, or by following incorporation of nucleotide analogues into nascent DNA.
Proteins were visualized by chemiluminescent detection using the ECL detection kit (Enhanced Chemiluminescence, Amersham) and films were digitized and analyzed using the Bio 1D software.
The immunoreactivity was visualized by chemiluminesecence detection following the manufacture's instruction (ECL Advance Western Blot detection Kit, Amersham).
Results were visualized by chemiluminescence detection using an ECL Kit (Millipore, USA) on Image Station 4000 MM Pro (Carestream Health Inc., USA).
Proteins of interest were visualized by chemiluminescent detection on an ImageQuant LAS mini4000 (GE Healthcare).
EGFP-labeled neurons were visualized by direct detection of endogenous fluorescence.
After sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and electroblotting, the biotinylated proteins were visualized by colorimetric detection following binding by streptavidin-alkaline phosphatase (streptavidin-AP).
Proteins were visualized by ECL detection system (Perbio Science) using anti-rabbit or anti-mouse HRP-conjugated IgG (Bio-Rad, Marnes La Coquette, France).
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