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By immunofluorescence and intravital microscopic studies, we found the interaction of MSC with the endothelium of blood vessels.
In addition to characterizing the SiNP ODN conjugates by a series of spectroscopic and microscopic studies, we have for the first time demonstrated that SiNP DNA conjugates can serve as fluorescence ON sensors that detect oncogenic miR-21.
Interestingly, from both the microscopic studies we found that SMAR1 induced the cells to exhibit smooth topography compared to rough surface profiles of either control or SMAR1-siRNA treated cells.
Employing immunofluorescence and electron microscopic studies we could now show for the first time in an in vitro model of the BCSFB that PMN can traverse epithelial monolayers transcellularly.
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On the basis of electron microscopic studies and other data, we propose that this is due to molecular bridging of the curvature by DivIVA multimers.
From these morphological, microscopic and immunohistochemical studies, we concluded that lens-specific expression of dnBrg1 disrupted proper fiber cell organization and suture formation, which impaired the optical quality of transgenic lenses and contributed to progressive cataract formation.
With electron microscopic studies using the tracer HRP (horse radish peroxidase) we demonstrated that the PPE is associated with increased transcytotic transport.
In one step further, we directly showed evidences by scanning electron microscopic studies that, all the three antibiotics formed some specific three-dimensional structures when conjugated with Gnps.
Microscopic studies were done under the light microscope (Olympus BH2) at 40X magnification.
Microscopic studies would reveal their existence while standard culture tests would show they had a different biochemistry from standard lifeforms.
However, microscopic studies of the eggshells have shown that they were not ceratopsian but theropod.
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