We report a general method based on wide-field fluorescence imaging of single molecule photobleaching and the Chung-Kennedy algorithm to measure the stoichiometry of functional protein complexes in living bacterial cells
Membrane proteins are often observed as higher-order oligomers, and in some cases in multiple stoich...
Full insight into the mechanisms of living cells can be achieved only by investigating the key proce...
Cellular processes result from dynamic interactions between biomolecules. The gold standard method f...
We report a general method based on wide-field fluorescence imaging of single molecule photobleachin...
We report here an image-based method to quantify the stoichiometry of diffraction-limited sub-cellul...
AbstractWe report here an image-based method to quantify the stoichiometry of diffraction-limited su...
We describe a method to detect molecular complexes and measure their stoichiometry in living cells f...
The brightness measured by fluorescence fluctuation spectroscopy specifies the average stoichiometry...
Fluorescence antibunching is a well-known technique for determining the number of independent emitte...
<div><p>The brightness measured by fluorescence fluctuation spectroscopy specifies the average stoic...
We developed in situ single cell pull-down (SiCPull) of GFP-tagged protein complexes based on microp...
ABSTRACT Imaging of fluorescence resonance energy transfer (FRET) between fluorescently labeled mole...
Single-molecule fluorescence imaging is often incompatible with physiological protein concentrations...
Summary: Single-molecule fluorescence recovery after photobleaching (smFRAP) is a newly developed te...
In the last two decades emerging single-molecule fluorescence tools have been developed and adapted ...
Membrane proteins are often observed as higher-order oligomers, and in some cases in multiple stoich...
Full insight into the mechanisms of living cells can be achieved only by investigating the key proce...
Cellular processes result from dynamic interactions between biomolecules. The gold standard method f...
We report a general method based on wide-field fluorescence imaging of single molecule photobleachin...
We report here an image-based method to quantify the stoichiometry of diffraction-limited sub-cellul...
AbstractWe report here an image-based method to quantify the stoichiometry of diffraction-limited su...
We describe a method to detect molecular complexes and measure their stoichiometry in living cells f...
The brightness measured by fluorescence fluctuation spectroscopy specifies the average stoichiometry...
Fluorescence antibunching is a well-known technique for determining the number of independent emitte...
<div><p>The brightness measured by fluorescence fluctuation spectroscopy specifies the average stoic...
We developed in situ single cell pull-down (SiCPull) of GFP-tagged protein complexes based on microp...
ABSTRACT Imaging of fluorescence resonance energy transfer (FRET) between fluorescently labeled mole...
Single-molecule fluorescence imaging is often incompatible with physiological protein concentrations...
Summary: Single-molecule fluorescence recovery after photobleaching (smFRAP) is a newly developed te...
In the last two decades emerging single-molecule fluorescence tools have been developed and adapted ...
Membrane proteins are often observed as higher-order oligomers, and in some cases in multiple stoich...
Full insight into the mechanisms of living cells can be achieved only by investigating the key proce...
Cellular processes result from dynamic interactions between biomolecules. The gold standard method f...