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Benjamin Flottmann

Researcher at Heidelberg University

Publications -  9
Citations -  325

Benjamin Flottmann is an academic researcher from Heidelberg University. The author has contributed to research in topics: Super-resolution microscopy & Microscopy. The author has an hindex of 9, co-authored 9 publications receiving 299 citations. Previous affiliations of Benjamin Flottmann include Goethe University Frankfurt.

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Chemically Induced Photoswitching of Fluorescent Probes—A General Concept for Super-Resolution Microscopy

TL;DR: Fluorescence probes that can be photoswitched or photoactivated and are suited for single-molecule localization based super-resolution microscopy are reviewed, and mEos2 is identified as a fluorescent protein that exhibits reversible photoswitching under various imaging buffer conditions.
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Three-Dimensional, Tomographic Super-Resolution Fluorescence Imaging of Serially Sectioned Thick Samples

TL;DR: TomoSTORM, an approach combining single-molecule localization-based super-resolution microscopy with array tomography of structurally intact brain tissue, delineated the course of the membrane and fine-structure of mitochondria in large tissue volumes with a resolution three orders of magnitude better than confocal microscopy.
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Single‐molecule super‐resolution imaging by tryptophan‐quenching‐induced photoswitching of phalloidin‐fluorophore conjugates

TL;DR: The nanoenvironment of fluorophores within a probe can be advantageously used to induce particular properties such as light‐induced photoswitching and single‐molecule super‐resolution imaging for various fluorophore‐phalloidin conjugates in aqueous buffer without the addition of further chemicals.
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Kar1 binding to Sfi1 C-terminal regions anchors the SPB bridge to the nuclear envelope

TL;DR: Kar1 interacts with the C-terminal (CT) region of Sfi1 to tether the yeast centrosome’s bridge to the nuclear envelope; Sfi 1-CT and C- terminal Cdc31-binding regions form the antiparallel Sfi2 overlap in the bridge.
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Correlative light microscopy for high-content screening.

TL;DR: This work introduces correlative light microscopy by combining fast automated widefield imaging, confocal microscopy and super-resolution microscopy, and demonstrates the potential of this approach for scalable experiments.