Currently, the most effective way of obtaining morphological information about LDs and their interaction with other subcellular organelles and structures is by electron microscopy, preferably by combining high pressure freezing (HPF) with electron tomography.
Taken together with the results from super-resolution fluorescence microscopy, these data suggest that by combining fluorescence microscopy modalities it may be possible to monitor Aβ on-cell aggregation on the single molecule level in real time.
By combining microscopy, spectroscopy, and a little bit of AI, the Verifier compares what it sees to a known version of the item and tells you whether they're the same.
By using crystalline specimens, x-ray diffraction and cryoelectron microscopy overcome these limitations by combining information from many (n) identical units, increasing the signal by a factor of n or (equivalently) spreading the damage over n molecules.
Significant progress toward the establishment of a method for cell density estimation based on light microscopy images was made by combining confluency measurements with texture analysis.
This has recently become possible by using an integrated laser and electron microscope (iLEM) as a chemical imaging method, as demonstrated by Karreman and co-workers, and by combining fluorescence microscopy with Focused Ion Beam-Scanning Electron Microscopy (FIB-SEM) imaging, as explored by Buurmans, De Winter, and co-workers.
Kazemifar et al. (2016) quantified the flow dynamics of the scCO2 displacement of water in a 2D porous micromodel by combining fluorescence microscopy and microscopic particle image velocimetry (PIV).
The chemical compositions of the AuPd alloyed NPs have been investigated by combining electron microscopy dispersive X-ray analysis, X-ray photoelectron spectroscopy and surface oxygen desorption using electrochemical reduction of catalysts.
