In
FRAP assays (FRAP: Fluorescence Recovery After Photobleaching), the time that fluorescent molecules need to replenish a bleached - out area is measured,...
In
FRAP assays, the time that fluorescent molecules need to replenish a bleached - out area is measured, basically assessing how quickly a dark sample area turns bright again.
In the journal Nature Communications they call attention to the limitations of pre-existing analysis tools for
FRAP assays — and offer a flexible and accurate alternative: their open - access software «PyFRAP.»
Joao Firmino (Knust, MPG)-- «
A FRAP assay to determine the influence of Crumbs in membrane protein dynamics» (2011)
Pick some of the foods from
the FRAP assay and start building up your antioxidant capabilities.
A study conducted at the University of Oslo in Norway compiled 3,100 food items using
the FRAP assay method of measurement, which extracts the antioxidant value of foods and beverages with the scale of millimoles / 100 grams.
The ferric reducing ability of plasma (FRAP) as a measure of «antioxidant power»:
the FRAP assay.
Not exact matches
With the availability of a more precise analysis method, new applications for
FRAP or iFRAP
assays could now arise.
Scientists are therefore using so - called «
FRAP»
assays (
FRAP: Fluorescence Recovery After Photobleaching) to investigate diffusion kinetics, a method established more than 40 years ago.
The Fluorescence Recovery After Photobleaching (
FRAP)
assay has been used to validate many of the SGC's chemical probes against bromodomains.
Scientists are therefore using so - called «
FRAP»
assays to investigate diffusion kinetics, a method established more than 40 years ago.
JQ1 inhibits recruitment and binding of Brd4 to TNFα and E-selectin promoter elements, and accelerates recovery time in
FRAP (fluorescence recovery after photobleaching)
assays using GFP - Brd4.
The histone deacetylase (HDAC) inhibitor suberoylanilide hydroxamic acid (SAHA) was used to increase overall levels of histone acetylation, resulting in a sufficient
assay window to enable the measurement of differences in recovery time and demonstrating the acetylation dependence of the
FRAP experiments.
I think the 3100 was a modified
FRAP... When there are different
assays all you can really do is intra-assay comparisons.