Journal: BioMed Research International

Article Title: Nonuniform Internal Structure of Fibrin Fibers: Protein Density and Bond Density Strongly Decrease with Increasing Diameter

doi: 10.1155/2017/6385628

Figure Lengend Snippet: Experimental setup of fluorescence intensity measurement. (a) Schematic lateral view of setup. The AFM is above the sample, and the objective lens of the inverted fluorescence microscope is below the sample. ((b), (c)) Fluorescence images of fibrin fibers. (d) AFM topography image of the same region (yellow box) of fibrin fibers as in (c). (e) Fluorescence intensity distribution of the cross-section (along the red line in (c)) of a single fiber; total fluorescence intensity of this fiber corresponds to the area under this curve. (f) Height distribution of the cross-section along the red line of the fiber in (d), which is the same fiber as in (c). Even though the fiber in (c) looks very bright, it was far below saturation as the gray value limit is 16384 (2 14 ).

Article Snippet: We used an inverted fluorescence microscope (Axiovert 200 or Observer D, Zeiss, Göttingen, Germany) in these experiments.

Techniques: Fluorescence, Microscopy