Results 11 to 20 of about 40,790 (312)

FRAP analysis: accounting for bleaching during image capture. [PDF]

open access: yesPLoS ONE, 2012
The analysis of Fluorescence Recovery After Photobleaching (FRAP) experiments involves mathematical modeling of the fluorescence recovery process. An important feature of FRAP experiments that tends to be ignored in the modeling is that there can be a ...
Jun Wu   +3 more
doaj   +4 more sources

Fluorescence recovery after photobleaching (FRAP) v1 [PDF]

open access: gold, 2022
This protocol details methods of the FRAP analysis of LRRK2-induced liposome tubules in vitro
Xinbo Wang
openalex   +2 more sources

Parameter identifiability in PDE models of fluorescence recovery after photobleaching [PDF]

open access: greenBulletin of Mathematical Biology, 2023
Identifying unique parameters for mathematical models describing biological data can be challenging and often impossible. Parameter identifiability for partial differential equations models in cell biology is especially difficult given that many established \textit{in vivo} measurements of protein dynamics average out the spatial dimensions.
Maria-Veronica Ciocanel   +6 more
openalex   +5 more sources

Defining the Diffusion in Model Membranes Using Line Fluorescence Recovery after Photobleaching [PDF]

open access: yesMembranes, 2020
In this study, we explore the use of line FRAP to detect diffusion in synthetic lipid membranes. The study of the dynamics of these membrane lipids can, however, be challenging.
Jakob L. Kure   +4 more
doaj   +2 more sources

Protein Synthesis Rate Assessment by Fluorescence Recovery after Photobleaching (FRAP) [PDF]

open access: yesBio-Protocol, 2017
Currently available biochemical methods cannot be applied to monitor protein synthesis in specific cells or tissues, in live specimens. Here, we describe a non-invasive method for monitoring protein synthesis in single cells or tissues with intrinsically
Nikos Kourtis, Nektarios Tavernarakis
doaj   +2 more sources

Determination of diffusion coefficient by image-based fluorescence recovery after photobleaching and single particle tracking system implemented in a single platform

open access: goldJournal of Innovative Optical Health Sciences, 2021
Fluorescence recovery after photobleaching (FRAP) and single particle tracking (SPT) techniques determine the diffusion coefficient from average diffusive motion of high-concentration molecules and from trajectories of low-concentration single molecules,
Donghee Lee   +2 more
doaj   +2 more sources

Long-term molecular turnover of actin stress fibers revealed by advection-reaction analysis in fluorescence recovery after photobleaching. [PDF]

open access: yesPLoS ONE, 2022
Fluorescence recovery after photobleaching (FRAP) is a versatile technique to evaluate the intracellular molecular exchange called turnover. Mechanochemical models of FRAP typically consider the molecular diffusion and chemical reaction that ...
Takumi Saito   +2 more
doaj   +2 more sources

Single- and two-photon fluorescence recovery after photobleaching. [PDF]

open access: yesCold Spring Harb Protoc, 2015
Fluorescence recovery after photobleaching (FRAP) is a microscopy technique for measuring the kinetics of fluorescently labeled molecules and can be applied both in vitro and in vivo for two- and three-dimensional systems. This introduction discusses the three basic FRAP methods: traditional FRAP, multiphoton FRAP (MPFRAP), and FRAP with spatial ...
Sullivan KD, Majewska AK, Brown EB.
europepmc   +4 more sources

Analysis of Active Transport by Fluorescence Recovery after Photobleaching. [PDF]

open access: yesBiophys J, 2017
Fluorescence recovery after photobleaching (FRAP) is a well-established experimental technique to study binding and diffusion of molecules in cells. Although a large number of analytical and numerical models have been developed to extract binding and diffusion rates from FRAP recovery curves, active transport of molecules is typically not included in ...
Ciocanel MV   +4 more
europepmc   +4 more sources

Assessing cellular efficacy of bromodomain inhibitors using fluorescence recovery after photobleaching. [PDF]

open access: yesEpigenetics Chromatin, 2014
BACKGROUND: Acetylation of lysine residues in histone tails plays an important role in the regulation of gene transcription. Bromdomains are the readers of acetylated histone marks, and, consequently, bromodomain-containing proteins have a variety of ...
Philpott M   +9 more
europepmc   +4 more sources

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