Caption Confocal microscopy 3D images of adhesive tape with paper backing; the adhesive layer of the tape is in red, while the paper backing is invisible; a gel filled with the nanostructured ...

The rapid proliferation of complex 3D cell and tissue culture models ... this configuration enables rapid acquisition of high-quality confocal images through hundreds of micrometers of air ...

An SEM can yield remarkably detailed 3D images of the tiniest structures ... The basic scheme here is known as confocal laser scanning fluorescence microscopy, where a laser at one wavelength ...

A confocal microscope is a kind of fluorescent microscope used to obtain high-quality 2D and 3D images. The device is most commonly used to view cells and cell structures, but can be used to ...

Here, we introduce a one-shot, high-multiplexing workflow on the STELLARIS confocal platform for 3D imaging of mouse tumor ... followed by registering the images and repositioning the sample ...

Fig. 1: Confocal microscopy images of lipid vesicles containing two different fluorescent dyes: (a) Two vesicles before fusion (equatorial section); (b) Vesicles fused by applying a short electric ...

The Confocal Microscopy and Image Analysis Core provides instrumentation and expertise to support the acquisition, processing and analysis of both fluorescence and bright-field micrographs captured ...

In confocal microscopy, laser light is focused into a very small spot and is scanned across the specimen to reconstitute a 2D image. This is in contrast to wide-field microscopes in which the entire ...

This 3D-printed confocal laser scanning microscope is a ... rather than getting an image of all the points within a two-dimensional focal plane, the scanning function moves the focal point around ...

Two digital cameras are mounted on this system: a Photometrics CoolSNAP HQ2 CCD camera for high-resolution imaging and an Photometrics Evolve 512 EMCCD camera for fast acquisition, ideal for 3D live ...

Optimized optical components enable Raman spectra to be recorded at each image pixel with acquisition times on the order of milliseconds. Due to the confocal setup, it is not only possible to collect ...

Aim: This study examines the absolute quantification of particle uptake into cells. Methods: We developed a novel method to analyze stacks of confocal fluorescence images of single cells ...