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Subcellular localization in leaf tissues was examined by confocal laser scanning light microscopy.
In vitro and in vivo evaluations were performed using several techniques, namely confocal scanning light microscopy analysis, rheometry, Gamma scintigraphic technique and microdialysis method.
We modified Costerton's techniques to examine biofilm via confocal scanning light microscopy on the peritoneal catheter [ 45].
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Reconstructions of zebrafish early embryonic development by scanned light sheet microscopy provide a 'digital embryo' with a database of cell positions, divisions and migratory tracks [18].
To observe branchiomotoneuron migration and axon outgrowth in real time, Isl-l GFP fIsl-l GFPimaged by digital scanned light sheet microscopy (DSLM) between 24–36 hpfish
> -wrap-foot> Wevaluatete our approach in scanned light-sheet microscopy datasets.
To determine the MVD, sections were scanned under light microscopy at low power (× 100), and three most vascular areas (vascular hot spots) were chosen.
The immunostained sections were scanned by light microscopy, and all of the tumor cells were evaluated: -, negative; +, focal expression < 5% of cancer tissues; + +, focal expression in 5 20% of cancer tissues; and + + +, diffuse expression > 20% of cancer tissues.
Thermal stability and microstructure were studied by differential scanning calorimetry (DSC), light microscopy, scanning electron microscopy (SEM) with energy-dispersive spectrometry (EDS) and X-ray diffraction (XRD).
Confocal laser scanning and light microscopy of A. thaliana and N. tabacum cells revealed that okadaic acid arrested cell growth, alter cell morphology, and affected the organization of microtubules.
Ultrastructural and histological adaptations of the rumen epithelium were imaged by scanning electron and light microscopy.
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