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. Internalised FM4-64 is rapidly transferred to vesicles containing Syb1. (A) Endocytosed FM4-64 (red) is rapidly transferred to Syb1 vesicles (green) as judged by the overlap of the two signals (yellow) after less than 1 minute. This series shows a pre-NETO cell. Note that Syb1 vesicles at the non-growing new end remain green. (B) Ratio of green and red fluorescence at the old (O) and new (N) ends pre and post NETO. In pre-NETO cells, FM4-64 uptake (red bars) is confined to the old end despite there being a bias to Syb1 vesicles (green bars) at the opposite pole. In post-NETO cells the two poles are equivalent. Error bars indicate s.e.m. Bar, 10 µm.





Right arrow Return to article