Results 51 to 60 of about 6,539 (187)

High-throughput fluorescence lifetime imaging flow cytometry

open access: yesNature Communications
Flow cytometry is a vital tool in biomedical research and laboratory medicine. However, its accuracy is often compromised by undesired fluctuations in fluorescence intensity.
Hiroshi Kanno   +23 more
doaj   +1 more source

The Nature of Cell‐Penetrating Poly(disulfide)s

open access: yesAngewandte Chemie, EarlyView.
The mode of action of cell‐penetrating poly(disulfide)s (CPDs) is elucidated to understand thiol‐mediated uptake (TMU) in general and guide future efforts to control cellular entry for chemicals delivery and pathogen defense. ABSTRACT Cell‐penetrating poly(disulfide)s (CPDs) are the most popular thiol‐mediated uptake (TMU) tools for delivering attached
Saidbakhrom Saidjalolov   +7 more
wiley   +2 more sources

Rapid fluorescence lifetime imaging microscopy via few-photon imaging

open access: yesAPL Photonics
Conventional fluorescence lifetime imaging microscopy (FLIM) based on time-correlated single photon counting has great potential in various domains, notably in cellular biology, enabling comprehensive studies encompassing spatiotemporal dynamics and ...
Ming-Jie Sun   +5 more
doaj   +1 more source

In vivo melanin 3D quantification and z-epidermal distribution by multiphoton FLIM, phasor and Pseudo-FLIM analyses

open access: yesScientific Reports, 2022
Characterizing melanins in situ and determining their 3D z-epidermal distribution is paramount for understanding physiological/pathological processes of melanin neosynthesis, transfer, degradation or modulation with external UV exposure or cosmetic ...
Ana-Maria Pena   +6 more
doaj   +1 more source

Imaging mitochondrial membrane potential via concentration-dependent fluorescence lifetime changes

open access: yesNature Communications
Mitochondria are central to cellular metabolism. Various fluorescence tools have been developed for imaging the mitochondrial environment. Yet, new reporters and imaging methods for directly reading the mitochondrial status are needed for high spatial ...
Dilizhatai Saimi   +12 more
doaj   +1 more source

Characterization of SPAD Array for Multifocal High-Content Screening Applications

open access: yesPhotonics, 2016
Current instruments used to detect specific protein-protein interactions in live cells for applications in high-content screening (HCS) are limited by the time required to measure the lifetime.
Anthony Tsikouras   +5 more
doaj   +1 more source

Luminescent probes for luminescence lifetime sensing and imaging in live cells: a narrative review

open access: yesJournal of Bio-X Research, 2020
. Luminescence (mostly fluorescence and phosphorescence) probes are a powerful tool widely used in the life sciences research. They can be used, for example, in the quantitative analysis of physiological parameters, visualization of different cell ...
Kaixuan Nie   +4 more
doaj   +1 more source

A fluorescence lifetime separation approach for FLIM live‐cell imaging

open access: yesJournal of Microscopy
Abstract Fluorescence lifetime imaging microscopy (FLIM) translates the duration of excited states of fluorophores into lifetime information as an additional source of contrast in images of biological samples.
Cornelia Wetzker   +8 more
openaire   +2 more sources

Platycodon grandiflorus–Derived Nanovesicles Sensitize Gastric Cancer to T Cell Killing via Ferroptosis‐Driven Membrane Mechanical Remodeling

open access: yesAdvanced Science, EarlyView.
Plant‐derived nanovesicles from Platycodon grandiflorus act as bioactive lipid delivery platforms that transport γ‐linolenic acid into gastric cancer cells. This lipid cargo promotes ferroptotic lipid peroxidation, remodels membrane mechanics, and increases tumor‐cell susceptibility to cytotoxic T‐cell attack.
Jian Wu   +9 more
wiley   +1 more source

Enhancing STED microscopy via fluorescence lifetime unmixing and filtering in two-species SPLIT-STED

open access: yesMethods in Microscopy
Simultaneous super-resolution imaging of multiple fluorophores remains a major challenge in STimulated Emission Depletion (STED) microscopy due to spectral overlap of STED-compatible fluorophores.
Deschênes Andréanne   +8 more
doaj   +1 more source

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