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. 2013 Jun 13;9(6):e1003095. doi: 10.1371/journal.pcbi.1003095

Figure 2. A: FRAP microscopy of fluorescently labeled Fab fragments of IgG.

Figure 2

For a typical FRAP experiment performed on a fibrin network, the regions of interest (ROIs, radius of 27 Inline graphicm) before, immediately after photobleaching, and after 98 s are shown (green circle). Normalized fluorescence recovery for the corresponding ROIs and their fits according to a model (Equation (7), ) are shown by symbols and a line, respectively. Fluorescence intensity values before (Inline graphic) and after (Inline graphic) photobleaching, and at the end of the experiment (I), are shown. For each sample, FRAP measurements were repeated 3 times in 8 different locations over the sample and the arithmetic mean of the intensity curves was taken. B: Hydrodynamic diameter measurements by dynamic light scattering: circles denote Inline graphic-thrombin and squares denote Fab IgG.