Azat Sharipov

TL;DR: Multiplane 3D SOFI is demonstrated by imaging fluorescently labelled cells over an imaged volume of up to 65 × 65 × 3.5 μm3 without depth scanning and shows that the depth sampling can be increased.

TL;DR: In this article, a combination of a label-free white light quantitative phase imaging with fluorescence to provide high-speed imaging and spatial super-resolution was proposed for cellular and subcellular structures.

TL;DR: This PALM-SOFI concept provides an enlarged quantitative imaging framework, allowing unprecedented functional exploration of focal adhesions through the estimation of molecular parameters such as fluorophore densities and photoactivation or photoswitching kinetics.

TL;DR: This tool incorporates SOFI and STORM algorithms, displays and describes the SOFI image processing steps in a tutorial-like fashion and demonstrates the performance of the simulation tool by comparing simulated results with experimentally acquired data.

TL;DR: In this paper, a combination of a novel label-free white light quantitative phase tomography with fluorescence imaging was proposed to provide high-speed imaging and spatial super-resolution, which allowed to not only image live cells in 3D at up to 200 Hz, but also integrate fluorescence superresolution optical fluctuation imaging within the same optical instrument.