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Electron microscopy allows for higher magnifications.
Modern electron microscopy allows for atomic resolution images of crystalline structures [1].
X-ray microscopy allows for high resolution imaging of X-ray transmission, with near 10 nm spatial resolution achievable today (Rehbein et al. 2009).
Light microscopy allows for kinetic observations in living cells; in particular, modern fluorescence technology affords imaging of single fluorophores with high temporal resolution.
Harmonic optical microscopy allows for the observation of fresh atrial tissue directly without staining and for obtaining sequential images by scanning the whole depth of the material.
Together, CARS microscopy allows for the assaying of various aspects of fat storage in living C. elegans in a non-invasive and label-free manner.
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We conclude that the FlowCAM is less tedious and time-consuming than microscopy, allowing for examination of more cells for greater counting precision.
This hypothesis relies on recent progresses in imaging technologies such as fluorescence confocal microscopy, allowing for the first time the identification of each chromosome-specific chromatin during interphase.
Within the purview of membrane proteins and ligand gated ion channels (LGICs), these outstanding advances in single molecule microscopy allow for the direct observation of discrete biochemical states and their fluctuation dynamics.
In situ electrochemical studies using atomic force microscopy allow for the direct observation of the morphology of the Li-ion battery cathode, at a nanometer scale resolution, during the cycling of an electrochemical cell.
In the other two recent studies [3,4], total internal reflection fluorescent microscopy allowed for imaging of the dynamics of the ESCRT machinery at the site of viral budding.
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