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Cells were then mixed with Alamar Blue dye to determine viability (expressed as mean relative fluorescence).
Data were expressed as mean relative fluorescence intensity (MFI) of 3000 cells.
Fluorescence ratios were calculated from the mean relative fluorescence intensities over a section delineated through each IB.
The mean relative fluorescence of non-normally pigmented, inflamed Porites massive tissue (fig. 4a) was significantly higher than that of healthy tissue (T (2) = 13.0067, P = 0.05).
For gel quantification and spiking reactions, each sample was normalized to 4R tau, and the data is presented as mean relative fluorescence or mean relative tau aggregation ± SEM.
Fig. S3: Mean relative fluorescence intensities of DNA-hexaploid, DNA-heptaploid, DNA-octoploid and DNA-enneaploid samples of Senecio carniolicus.
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The phagocytic index (PI) defined as the percentage of cells with internalized fluorescence × the mean relative fluorescent units internalized per cell (RFU/cell) was calculated as previously described (Gauthier et al., 2010).
The relative binding for each glycan was expressed as mean RFU (relative fluorescence units) of four of the six replicates.
The lag time for each molecule was defined as the last read at which the fluorescence was equal to or above the lower bound of a 95% confidence interval for the mean starting relative fluorescence.
The means of relative fluorescence intensity to H3 are shown in the graphs.
The means of relative fluorescence intensity to H3 is shown in the graphs.
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mean relative amplitude
mean relative difference
mean relative baseline
mean relative impact
mean relative percentage
mean relative percent
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mean relative prediction
mean relative importance
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mean relative error
mean relative tumor
mean relative humidity
mean relative branch
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