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This eliminates the need to stain with lectins or antisera to visualize the cells, and therefore allows the cells to be visualized simultaneously with other structures in the developing kidney by combined immunohistochemistry/GFP detection.
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In contrast to previous CARS studies of brain tissue, different biological structures were visualized simultaneously and separated from each other by different colors.
Both bone and soft-tissue lesions can be visualized and identified with greater and more convincing accuracy.
The plates were visualized first with UV illumination followed by charring with ninhydrin (0.3% ninhydrin (w/v), 97 3 EtOH-AcOH).
Reaction products were visualized following incubation with diaminobenzidine (DAB) and then counterstained with hematoxylin.
Protein bands were visualized with Western Lightning ECL (Perkin Elmer) and detected with a luminescent image analyzer LAS-30000, FujiFilm).
The bands were detected by chemiluminescence using the SuperSignal West Dura Chemiluminescent Substrate (Thermo); images were visualized and acquired with ChemiDoc XRS+ System and Image Lab software (Bio-Rad).
Attached cells are visualized with crystal violet staining.
The resulting network components were visualized and analyzed with Cytoscape.
Protein structures were visualized and aligned with MacPyMOL.
The ethidium bromide stained PCR products were visualized following illumination with UV light.
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