To maximize the sensitivity of co-localization analysis and fully exploit the resolution of the microscope objective (Zeiss 63X oil immersion objective NA = 1.4), we used a 3.0 scan zoom so that each pixel covered 0.05 μm.
All samples were included and batch processed using a zoom scan filter, three steps peak detector (local maxima mass detection, score connector chromatogram construction, Savitzky-Golay peak recognition) and alignment join aligner.
Hoping to gain some insight into how to restore these delicate objects, a team of researchers used a scanning electron microscope to zoom in on the surface of daguerreotypes and discovered life.
SPECT images were acquired using a 1.5X zoom, 128 × 128 matrices, and a step and-shoot step and-shoot
The LCQ-DECA was operated in data-dependent acquisition mode, using a survey scan of 400 1500 m/z, a data-dependent zoom scan, and MS/MS of singly, doubly and triply charged ions.
Stochastic distribution of 10-μm beads was confirmed using a stereo zoom microscope.
Just after inoculation, macroscopic images were acquired using a fluorescence zoom microscope.
Tumor growth and vessels were observed daily using a SZ61 Zoom Stereo Microscope (Olympus, Tokyo, Japan).
Bands of PCR-amplified products were scanned and analysed semiquantitatively, using a zoom digital camera (DC290) with an EDAS 290 imaging system (Kodak, Rochester, NY, USA).
To maintain both high resolution and fast scan speed, images were acquired using a zoom factor of 3.5× and were clipped as close to the soma as reasonably possible.
