Differential fluorescence labeling and multi-fluorescence imaging followed by colocalization analysis is commonly used to investigate cellular heterogeneity in situ. This is particularly important when investigating the biology of tissues with diverse cell types. Object-based colocalization analysis (OBCA) tools can employ automatic approaches, which are sensitive to errors in cell segmentation, or manual approaches, which can be impractical and tedious. Here, we present a novel set of tools for OBCA using a semi-automatic approach, consisting of two ImageJ plugins, a Microsoft Excel macro, and a MATLAB script. One ImageJ plugin enables customizable processing of multichannel 3D images for enhanced visualization of features relevant to OBCA...
AbstractBiomolecular interactions are fundamental to the vast majority of cellular processes, and id...
Analysis of multicellular patterns is required to understand tissue organizational processes. By usi...
Colocalizing two fluorescent-labeled proteins remains an open issue in diffraction-limited micro-sco...
The use of fluorescence microscopy to investigate protein colocalization is an invaluable tool for u...
Quantification of fluorescence colocalization and intensity of strongly overlapping cells, e.g., neu...
We are excited to announce the first official release of ColocalVision, a powerful and user-friendly...
AbstractAccurately localizing molecules within the cell is one of main tasks of modern biology, and ...
International audienceThe quantitative analysis of molecule interactions in bioimaging is key for un...
The subcellular localization of objects, such as organelles, proteins, or other molecules, instructs...
<p>(A) Double immunofluorescence analysis of FITC-labeled SNA-I (a, e, i and m), and marker for ER (...
ABSTRACT Biomolecular interactions are fundamental to the vast majority of cellular processes, and i...
Background and objective Extracting accurate information from complex biological processes involved ...
The qualitative analysis of colocalisation in fluorescence microscopy is of critical importance to t...
Blobs and curves occur everywhere in plant bioimaging: from signals of fluorescence-labelled protein...
Bioloc3D: an automatized and user-friendly toolset to quantify fluorescent profiles and their coloca...
AbstractBiomolecular interactions are fundamental to the vast majority of cellular processes, and id...
Analysis of multicellular patterns is required to understand tissue organizational processes. By usi...
Colocalizing two fluorescent-labeled proteins remains an open issue in diffraction-limited micro-sco...
The use of fluorescence microscopy to investigate protein colocalization is an invaluable tool for u...
Quantification of fluorescence colocalization and intensity of strongly overlapping cells, e.g., neu...
We are excited to announce the first official release of ColocalVision, a powerful and user-friendly...
AbstractAccurately localizing molecules within the cell is one of main tasks of modern biology, and ...
International audienceThe quantitative analysis of molecule interactions in bioimaging is key for un...
The subcellular localization of objects, such as organelles, proteins, or other molecules, instructs...
<p>(A) Double immunofluorescence analysis of FITC-labeled SNA-I (a, e, i and m), and marker for ER (...
ABSTRACT Biomolecular interactions are fundamental to the vast majority of cellular processes, and i...
Background and objective Extracting accurate information from complex biological processes involved ...
The qualitative analysis of colocalisation in fluorescence microscopy is of critical importance to t...
Blobs and curves occur everywhere in plant bioimaging: from signals of fluorescence-labelled protein...
Bioloc3D: an automatized and user-friendly toolset to quantify fluorescent profiles and their coloca...
AbstractBiomolecular interactions are fundamental to the vast majority of cellular processes, and id...
Analysis of multicellular patterns is required to understand tissue organizational processes. By usi...
Colocalizing two fluorescent-labeled proteins remains an open issue in diffraction-limited micro-sco...