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By using contact angle measurements and atomic-force microscopy studies, we estimate the degree of vertical phase separation in bulk heterojunctions.
Based on detailed transmission electron microscopy studies we show that the hexagonal phase fraction in (Al0.76Cr0.24 2O3 and (Al0.70Cr0.25Fe0.05 2O3 coatings correlates with the presence of small spherical Cr- and Fe-enriched macroparticles.
In electron microscopy studies, we found that p43 overexpression increases mitochondrial mass (Figure 4A).
By electron and confocal microscopy studies, we confirmed surface expression of nucleolin and its indirect association with intracellular actin cytoskeleton [3].
Using a combination of immunoblot analysis, fluorescence and immunofluorescence microscopy studies, we found that steady-state GFPu levels were not detectably different between R6/2 and non-R6/2 brain.
Given the evident differences in THK523 staining, the fluorescence microscopy studies we present herein demonstrate that THK523, even at the very high concentration of 100 μM, does not bind to non-PHF-tau aggregates.
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In contrast, in our immunoelectron microscopy study we did not observe plasma membrane associated RTN1A-IR in Purkinje cells (Fig. 6).
This is in accordance with our electron microscopy studies where we did not observe a reduced amount of autophagosomes in Phb2 pko mice, suggesting that the mTOR effect may be independent of influencing the level of autophagy.
Based on our spectroscopic ellipsometry and atomic force microscopy (AFM) studies we can suggest that the variation of the refractive index, which is significantly reduced in the visible range for ternary systems, is involved in the physical mechanism of the phenomenon.
Using high-resolution electron microscopy and mechanistic studies, we describe the effect of physicochemical properties of nanoparticles on epithelial cell uptake, how uptake differs between different alveolar epithelial cells within the human lung, and how native surfactant proteins can bind to nanoparticles and modify their uptake.
To get more information about the trafficking of Stx from endosomes to the Golgi we performed confocal microscopy studies.
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