Team:TU Eindhoven/Project/Characterization/Fluorescence Microscopy
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<h2>Fluorescence Microscopy</h2> | <h2>Fluorescence Microscopy</h2> | ||
- | <p>In addition to the FACS results a confocal microscope was used to visualize the fluorescent cells. FACS results confirmed that the DBCO-<sub>4</sub>-5/6-TAMRA molecules were clicked to the cells. The microscope assay was just an additional assay whose results could be used for presentations. In the following figures the images taken by the confocal microscope are shown. | + | <p>In addition to the FACS results a confocal microscope was used to visualize the fluorescent cells. FACS results confirmed that the DBCO-PEG<sub>4</sub>-5/6-TAMRA molecules were clicked to the cells. The microscope assay was just an additional assay whose results could be used for presentations. In the following figures the images taken by the confocal microscope are shown. |
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The intensity of the pixels in the figures below gives an indication of the amount of fluorescence. The black pixel (0) means no fluorescence at all, the white (1) one represents the maximum relative fluorescence. | The intensity of the pixels in the figures below gives an indication of the amount of fluorescence. The black pixel (0) means no fluorescence at all, the white (1) one represents the maximum relative fluorescence. |
Latest revision as of 11:58, 15 October 2014
Fluorescence Microscopy
In addition to the FACS results a confocal microscope was used to visualize the fluorescent cells. FACS results confirmed that the DBCO-PEG4-5/6-TAMRA molecules were clicked to the cells. The microscope assay was just an additional assay whose results could be used for presentations. In the following figures the images taken by the confocal microscope are shown.
The intensity of the pixels in the figures below gives an indication of the amount of fluorescence. The black pixel (0) means no fluorescence at all, the white (1) one represents the maximum relative fluorescence.