Sentence examples for microscopy is that from inspiring English sources

However, one main disadvantage of confocal microscopy is that reflectance signals are intrinsically non-specific.

The advantage of fluorescence microscopy is that it allows scientists to label and image specific proteins.

A disadvantage of using high-resolution microscopy is that samples must be milled down to a fraction of their original thickness, destroying part of the artefact.

The operating principle (and primary advantage) of 2P microscopy is that the location of absorption can be controlled by laser intensity.

The value of 2P microscopy is that it affords an unparalleled view of single‐cell spatiotemporal dynamics deep within intact tissues and organs.

A key feature of this model that distinguishes it from other experimental models of intravital fluorescence video microscopy is that we record in 2-photon confocal mode.

Another important observation provided by confocal microscopy was that fluorescence in the inner core of the fibres was always superior to the background intensity (Fig. 5-d and Fig. 5-e), indicating that CBDs may have penetrated into the fibre.

The major realization, enabled by phase contrast microscopy, was that the optical phase shift accumulated through a cell is linearly proportional to non-aqueous content or dry mass of the cell.

Inherently, the spatial resolution of electron microscopy is higher than that of optical methods.

The illumination and detection scheme in CSM microscopy is different from that in localization microscopy.

A novel implementation of structured illumination microscopy is presented that overcomes these issues.