As with the genotyping assays described above, Factor II prothrombin (FII) mutant genotyping results were also visualized either in real time or as an end-point assay.
The embryo itself could not be visualized either.
QDs were visualized either on the bead surface (e.g. Figure 1) or in cross sections (in this case the bead surface is visible as rim around beads, e.g. Figure 2 and Figure 3c).
The reaction products were visualized either by UV shadowing, or by autoradiography.
Staining was visualized either using a fluorescent inverted microscope (Olympus 1X71) with a monochrome ORCA R digital camera (Hamamatsu) or as for immunocytochemistry.
Further, to visualize either tall or large features as completely separate objects would, of course, require a much larger separation, ∼6 10 ri.
To assist manual inspection and analysis, each structure prediction can be visualized interactively, either as a separate model or as a superposition with the target using PyMOL (DeLano, http://www.pymol.org).org
The genes are organized into rough groupings and are visualized as either orange (p<0.05) or blue (p>0.05) depending on their significance level (Table S6).
Staining of extended chromatin with anti-PICH antibodies readily demonstrated colocalization of PICH with chromatin fibers, as visualized by either anti-BrdU antibodies or DAPI (Fig. 1a).
The P-labeled adducts are separated from nonmodified radiolabeled 3′,5′ nucleotides (pNps) by two-dimensional TLC, and the adducts are either visualized as a pattern of spots by autoradiography or seen as chromatographic peaks by HPLC with radioactive detection.
