spacer gif spacer gif spacer gif spacer gif spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    


Right arrow Help viewing high resolution images
Right arrow Return to article
(Downloading may take up to 30 seconds.
If the slide opens in your browser, select File -> Save As to save it.)

Click on image to view larger version.



Fig. 3. EB1 and its C-terminal binding partner APC co-purify with centrosomes. Centrosomes were purified from nocodazole-treated MDCK cells (a-o) or U-2 OS cells (a'-o'), stained for the centrosome markers {gamma}-tubulin (green in a-c,a'-c'), centrin (red in d-f,d'-f') or pericentrin (red in g-n,g'-n') and co-stained for APC (red in a-c,a'-c' and green in d-f,d'-f'), EB1 (green in g-j,g'-j') or p150Glued/dynactin (green in k-n,k'-n'). Most of the purified centrosomes contain APC and EB1 (white arrowheads in a-j,a'-j'). An example of a centrosome without APC is shown (black arrowhead in d-f). By contrast, most of the centrosomes have little p150Glued/dynactin (arrows in k-n,k'-n') or no p150Glued/dynactin (black arrowheads in k-n). Examples of centrosomes that contain p150Glued/dynactin are shown (white arrowheads in k'-n'). Purified MDCK (o) or U-2 OS (o') centrosomes are functional as measured by induction of MT aster formation in vitro (o,o'). Bar, 10 µm.





Right arrow Return to article