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. 2016 Aug 1;27(15):2423–2434. doi: 10.1091/mbc.E16-01-0057

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© 2016 Trexler et al. This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0).

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FIGURE 4: — PIP2, dynamins, and several BAR domain–containing proteins are transiently recruited to the exocytic site near the time of membrane fusion. Background-subtracted and normalized fluorescence intensity traces for each protein indicated. Top, average NPY-GFP signal for all events (N = 200) as a relative standard of time. The dashed line marks the zero time point. The mean fluorescence intensity is shown as a dark line, and the SE of the data set is shown in transparency behind the data for all traces. The dagger indicates that there is not a statistically significant shift in intensity at t = 0 relative to the beginning of the trace, determined using t tests in Supplemental Figure S6. If the SE is not visible, it is smaller than the line. N = 50 for dnm-1, 38 for dnm-2, 34 for amphiphysin, 41 for syndapin2, 45 for endophilinA2, 30 for PIP2-sensor, and 30 for farn-mCherry.