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Furthermore Lambert-Beer's law must be rewritten for the case of convergent illumination as is provided by a typical microscope.
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The axial dimension in a typical microscope is scanned either by moving the sample relative to the output optics of the system or by moving a lens within the optical system.
We adopt z R = 0.5 μm for a typical microscope objective.
Nearly 10000 nanoholes can be simultaneously monitored under the field of view of a typical microscope.
The core of our experimental setup reproduces a typical fluorescence microscope as illustrated in Fig. 1a.
Yet, under a typical optical microscope, neurons that are active and firing look much the same as their quieter counterparts.
Taking advantage of the multimodality of a typical CARS microscope, we investigate the cause of cell-to-cell variability during adipogenesis by imaging multiple cellular events simultaneously within single 3T3-L1 cells.
Combining fluorescent imaging with vibrational imaging, a typical CARS microscope is capable of monitoring multiple signals simultaneously.
Alternatively, these problems may be addressed by less costly methods on a typical widefield fluorescent microscope with minimal expression times, more restrictive bandpass filter technology, and the use of multiple fluorescent proteins that are more spectrally distinct from each other.
A typical transmission electron microscope (TEM) image of the nanoparticles formed is presented in Fig. 4.
A typical scanning electron microscope (SEM) image of the In2O3NCs is shown in Fig. 1. Figure 1 SEM images of In2O3NCs grown by direct oxidation of In with O2at 1000 °C with an average diameter of 500 nm.
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