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W闤l, S.,Windoffer, R., and Leube, R.E. 2005.
Dissection of keratin dynamics: different contributions of the actin and microtubule systems.
Eur. J. Cell Biol. 84:311-28.

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movie 1. Fluorescence recording (inverse presentation) of a peripheral region of a living SK8/18-2 cells detecting dynamics of HK18-YFP distribution. Recording intervals, 25 s.

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movie 2. Fluorescence recording (inverse presentation) of a lamellipodium of a living SK8/18-2 cells recording dynamics of HK18-YFP distribution. Recording intervals, 25 s.

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movie 3. Time-lapse fluorescence microscopy  (inverse presentation) of a segment of a long, axonal-like extension of a living SK8/18-2 cell detecting dynamics of HK18-YFP-containing particles. Recording intervals, 25 s.

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movie 4. Time-lapse fluorescence image recording (inverse presentation) of living SK8/18-2 cells that were treated with 100 然 nocodazole monitoring the reaction of HK18-YFP-labelled structures. Recording intervals, 30 s.

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movie 5. Time-lapse fluorescence microscopy (inverse presentation) of living SK8/18-2 cells detecting dynamics of HK18-YFP distribution in the presence of 30 然 latrunculin B. Recording intervals, 25 s.

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movie 6. Time-lapse fluorescence microscopy (inverse presentation) at high power of a living SK8/18-2 cell detecting dynamics of HK18-YFP distribution in the presence of 30 然 latrunculin. The segment was taken from the same recording that was used to prepare movie 5. Recording intervals, 25 s.

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movie 7. Time-lapse fluorescence microscopy (inverse presentation) of living SK8/18-2 cells detecting dynamics of HK18-YFP distribution after addition of 30 然 latrunculin and subsequent addition of 40 然 nocodazole. Recording intervals, 25 s.

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movie 8. Time-lapse fluorescence microscopy (inverse presentation) of living SK8/18-2 cells detecting dynamics of HK18-YFP distribution after addition of 40 然 nocodazole and subsequent addition of 30 然 latrunculin. Recording intervals, 25 s.