Otey - Images
| Figure 1 | Figure 2 | Figure 3 | Figure 4 |
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Figure 1. Palladin (in green) is concentrated in closely-spaced spots associated with contractile bundles of actin filaments (in red), in a cultured A7r5 vascular smooth muscle cell. |
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Figure 2. (Figures 2-4.) In cultured fibroblasts, three-color immunofluorescence staining is used to detect palladin (green), actin (blue) and VASP (red), which is a regulator of actin filament growth and a molecular partner for palladin. Note that palladin and VASP are detected in regularly-spaced dots along the actin filament bundles, and also at the ends of the bundles, where they attach to the plasma membrane on the lower surface of the cell. |
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Figure 3. (Figures 2-4.) In cultured fibroblasts, three-color immunofluorescence staining is used to detect palladin (green), actin (blue) and VASP (red), which is a regulator of actin filament growth and a molecular partner for palladin. Note that palladin and VASP are detected in regularly-spaced dots along the actin filament bundles, and also at the ends of the bundles, where they attach to the plasma membrane on the lower surface of the cell. |
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Figure 4. (Figures 2-4.) In cultured fibroblasts, three-color immunofluorescence staining is used to detect palladin (green), actin (blue) and VASP (red), which is a regulator of actin filament growth and a molecular partner for palladin. Note that palladin and VASP are detected in regularly-spaced dots along the actin filament bundles, and also at the ends of the bundles, where they attach to the plasma membrane on the lower surface of the cell. |




