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Based on the geometric means of each histogram in Figure 11, the mean cellular fluorescence intensity for FA-targeted micelles was approximately 2.16 and 1.35 times higher than those nontargeted micelles and free C6, respectively.
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In 50 cells with monoallelic TP53 loss per specimen, the mean corrected total cellular fluorescence for LC3 was twofold higher (range 1.5 3.0) in cells from Tnv-6 contactivatedtivated cultures than corresponding control cultures, n=3, P=0.04.
Treated cells showed a significant (1.7-fold; P=0.0084) increase in mean HER2-corrected total cellular fluorescence compared with mock-irradiated cells.
Cellular fluorescence was also quantified by the geometric mean (Gmean).
There is marked variation in the cellular fluorescence with the distribution showing a standard deviation of 0.68 relative to the mean.
The cellular fluorescence from this cell population was presented as histograms along with relevant statistical values such as geometric mean and coefficient of variance.
b Intensity of cellular fluorescence.
Figure 3 Measurement of cellular fluorescence and drug uptake.
The cellular fluorescence was measured with an NC-3000 image cytometer using NC-SlideA8 (ChemoMetec, Allerod, Denmark).
In this review, the mechanism of surface-enhanced cellular fluorescence imaging is discussed in view of metal-enhanced fluorescence.
In contrast, slices from mutant mice exhibited widespread cellular fluorescence immediately after opening the fluorescence shutter.
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