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Remarkably, Ranchoux and co-workers applied transmission electron microscopy, and correlative light and electron microscopy, providing unequivocal ultrastructural-level evidence of ongoing dynamic EndMT in PH samples.
Temporal release and removal of select proteins (AzTMBmCh) was triggered with the application of thrombin and monitored in real-time with confocal microscopy, providing a responsive handle for controlling matrix properties.
Now we found that for some metals this corrosion at the buried interface can be studied in situ by Scanning Kelvin Probe microscopy, providing the means to better develop strategies for counter acting this problem.
Crystal defects in a plastically deformed Mg Zn–Y alloy have been studied on the atomic scale using aberration-corrected scanning transmission electron microscopy, providing important structural data for understanding the material's deformation behavior and strengthening mechanisms.
We studied the structures of two Sec protein complexes in solution involved in tandem translocation steps by electron microscopy, providing direct structural evidence of the oligomeric state of SecA in the initiation of preprotein translocation.
Furthermore, TIEG1 and Runx2 protein were shown to co-localize in the nucleus of WT calvarial osteoblasts via confocal microscopy providing further support for the interaction of these two transcription factors in osteoblasts (Figure 8B).
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Microscopy provided information on macroscopic emulsion morphologies.
Scanning electron microscopy provided morphology and quantified fiber alignment.
Optical and electron microscopy provide evidence of interphase bond enhancement.
Online microscopy provides 2D projections of 3D crystal shapes.
Scanning electron microscopy provided further insight into the morphology and size details of the AgNPs.
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