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Cell-wall components can also be visualised by selective staining.
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These points can be visualised by different graphical representations.
The arterioles are too small to be visualised by angiography.
Spots were visualised by UV light or ninhydrin.
The phase and semi-crystalline morphologies are visualised by scanning electron microscopy and atomic force microscopy.
Finally, runoff dynamics were visualised by adding a dye to the run-on water.
Additionally, the flow patterns were visualised by using a rheoscopic fluid.
The distribution of cells throughout perfusion-seeded scaffolds was visualised by confocal microscopy.
Protein DNA complexes were visualised by autoradiography.
Specific binding was visualised by standard techniques.
Cell death was visualised by UV transillumination.
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