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By examining cell morphology under microscope, we found that ectopic expression of dominant-active ROCK released cells from DLC1-induced cytoskeletal collapse and cell shrinkage.
With the aid of a dissecting microscope we found the illumination of a fiber optic light sufficient for the visualization of the olfactory bulbs and central sulcus of the brain.
When GFP expression was compared between the different transgenic lines using the same settings on the confocal microscope, we found that the GFP signals were always lower in the transgenic U lines bearing the pGFP-ZAM sensor transgene than they were with the flipped-out transgenes.
As expected, by analyzing LC3 punctae in fluorescence microscope, we found that ISO-1 attenuated ConA-triggered autophagy formation.
Using a light microscope, we found that the cell size decreased and that cell aggregation was obviously reduced in the Rap + Dex group.
It should be noted that with the settings of our confocal microscope, we found that R is in a reasonable linear relationship with GSH concentrations.
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Keeping its axial standard deviation fixed at eight pixels, a typical value measured on our microscopes, we found that up to a lateral standard deviation of 2 3 pixels, results from plane-wise and 3D deconvolution are undistinguishable (Supplementary Fig. S5).
Between microscope and virtual microscopy we found 20 discordant estimations, 18 between plain and assisted virtual microscopy and 18 between microscopy and assisted virtual microscopy.
Through potentiostatic polarization and scanning electron microscope (SEM), we found that the current efficiency keeps nearly unchanged with sodium nitrite introduction to the solutions.
Moreover, from preliminary electron microscope observations, we found that the samples with M NRM/M IRM values of ~1 contain pyrrhotite crystals (TNZ03-04-65 and the03-15-57) and TNZ03-08-078-07 sample contains both magnetite and pyrrhotite crystals.
By analyzing cardiomyocyte ultrastructure using transmission electron microscope [14], we found numerous membrane whorls in the sarcoplasmic reticulum and in or immediately adjacent to mitochondria, and pleomorphic mitochondria with effaced cristae in samples from mice receiving IM at 50 and 100 mg/kg per day (Figure 2G, arrows), consistent with a previous report [14].
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