Examples of 'mean fluorescence intensity' in a sentence
Meaning of "mean fluorescence intensity"
Mean fluorescence intensity (MFI) is a measurement used in flow cytometry to quantify the average fluorescence signal emitted by a population of cells or particles. It provides information about the level or abundance of a specific fluorescent marker within a sample and is commonly used in research and diagnostic applications
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mean fluorescence intensity
Numbers in plots indicate mean fluorescence intensity.
The mean fluorescence intensity of labeled cells was quantified.
The results are expressed as mean fluorescence intensity.
Mean fluorescence intensity was determined using flow cytometry.
Negative control mean fluorescence intensity.
The mean fluorescence intensity values are depicted in the figure.
The data presented is the mean fluorescence intensity.
The mean fluorescence intensity is depicted.
Binding was measured by mean fluorescence intensity.
The mean fluorescence intensity and representative histograms are shown.
The data was presented as the mean fluorescence intensity.
The mean fluorescence intensity is obtained from three independent experiments.
Values are expressed as a percentage of initial mean fluorescence intensity.
Mean fluorescence intensity.
Values represent the relative mean fluorescence intensity of staining.
See also
Mean fluorescence intensity values after subtracting background fluorescence are shown.
Both percentage of cells and mean fluorescence intensity was estimated.
The mean fluorescence intensity of the resultant peak is plotted as channel number.
Results are expressed as percentage of control expression based on mean fluorescence intensity.
Each data point is the mean fluorescence intensity of three donors.
The data were analyzed by percent of the population responding and mean fluorescence intensity.
Cells were washed and the mean fluorescence intensity was measured as described above.
The average fibre coarseness could then be used to calibrate the mean fluorescence intensity.
M the mean fluorescence intensity of the three replicate measurements for the concentration involved.
Each data point is the a calculated mean fluorescence intensity of three donors.
The mean fluorescence intensity was then calculated for each ROI.
Numbers indicate percent positive cells and mean fluorescence intensity in parentheses.
Mean fluorescence intensity values were derived from a FACS analysis as described.
The level of receptor expression correlated with mean fluorescence intensity and high expressors were selected.
The mean fluorescence intensity of each sample was calculated using FACS Diva software.
As used herein MFI refers to mean fluorescence intensity.
Most commonly, mean fluorescence intensity in a region of interest is used.
The x axis is time in minutes and the y axis denotes Mean Fluorescence Intensity.
Figure 3 presents the mean fluorescence intensity fold increase above isotype control.
The data are expressed as % inhibition of mean fluorescence intensity.
The y-axis indicates the mean fluorescence intensity obtained for each composition used.
The abscissa represents the antibody concentration ( µg / ml ) and the ordinate represents the mean fluorescence intensity.
For example, a minimal mean fluorescence intensity may be established which predicts positive outcome.
Surface antigen expression was measured as the mean fluorescence intensity ratio ( MFIR ).
Mean fluorescence intensity was recorded as set forth in Table 2 hereafter.
For each flow cytometry graph, the mean fluorescence intensity corresponds to the median value.
Mean fluorescence intensity ( MFI ) was used as a unit of measure of antibody binding.
As the chemokine concentration increases, the mean fluorescence intensity for each group of beads increases.
Mean fluorescence intensity ( MFI ) is plotted for each antibody concentration used.
Results are expressed as mean fluorescence intensity ± SD of triplicate cultures.
Mean Fluorescence Intensity values are shown in Table 9 below.
Percentage of stained cells and mean fluorescence intensity ( MFI ) are indicated.
The mean fluorescence intensity ( MFI ) of phagocytic cells was then evaluated by flow cytometry.
Labelled antibody binding was determined as mean fluorescence intensity ( MFI ) by flow cytometry.
On day 4, mean fluorescence intensity is measured by flow cytometry.
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