Frap Analysis

FRAP analysis, or fluorescence recovery after photobleaching, is a live-cell imaging method used to measure the mobility and exchange of fluorescently labeled molecules. In a defined region, intense light temporarily bleaches fluorescence, and recovery is monitored as unbleached molecules move into the area or exchange with bleached molecules; recovery curves can indicate diffusion rates, mobile fractions, and molecular interactions. In bioengineering, FRAP analysis helps characterize membrane proteins, cytoskeletal components, biomaterials, and engineered tissues under controlled conditions. These measurements clarify how molecular transport and binding influence cellular organization, material performance, and the design of therapeutic or regenerative systems.

Frap Analysis - Related Videos

Research

JoVE Journal - Biology

Analysis of the Gap Junction-dependent Transfer of miRNA with 3D-FRAP Microscopy

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Cited by 6 •

2017

Here, we describe the application of three-dimensional fluorescence recovery after photobleaching (3D-FRAP) for the analysis of the gap junction-dependent shuttling of miRNA. In contrast to commonly applied methods, 3D-FRAP allows for the quantification of the intercellular transfer of small RNAs in real time, with high spatio-temporal resolution.

Photobleaching Assays (FRAP & FLIP) to Measure Chromatin Protein Dynamics in Living Embryonic Stem Cells

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Cited by 26 •

2011

We describe photobleaching methods including Fluorescence Recovery After Photobleaching (FRAP) and Fluorescence Loss In Photobleaching (FLIP) to monitor chromatin protein dynamics in embryonic stem (ES) cells. Chromatin protein dynamics, which is considered to be one of the means to study chromatin plasticity, is enhanced in pluripotent cells.

Research

JoVE Journal - Neuroscience
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Fluorescence Recovery After Photobleaching (FRAP) of Fluorescence Tagged Proteins in Dendritic Spines of Cultured Hippocampal Neurons

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Cited by 33 •

2011

FRAP has been used to quantify the mobility of Green Fluorescence Protein (GFP)-tagged proteins in cultured cells. We examined the mobile/immobile fractions of the GFP by analyzing the fluorescence recovery percentage after photobleaching. In this study, FRAP was performed at spines of hippocampal neurons.

Research

JoVE Journal - Biology
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A Neuronal and Astrocyte Co-Culture Assay for High Content Analysis of Neurotoxicity

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Cited by 46 •

2009

This article describes a novel protocol and reagent set designed for sensitive measurement of neurotoxic effects of compounds and treatments on co-cultures of neurons and astrocytes using high content analysis. Results demonstrate that high content analysis represents an exciting novel technology for neurotoxicity assessment.

Automated Analysis of Intracellular Phenotypes of Salmonella Using ImageJ

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Cited by 3 •

2022

Salmonella invades and replicates inside intestinal epithelial cells both in Salmonella-specific vacuoles and free in the cytosol (hyper-replication). A high-throughput fluorescence microscopy-based protocol is described here to quantify the intracellular phenotypes of Salmonella by two complementary image analyses through ImageJ, reaching single-cell resolution and scoring.

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