Video 2.

Sequential z sections (0.4-µm step size) of a prometaphase cell presented as a video generated in Volocity 5.5. A fixed Xenopus S3 cell stained for INCENP (blue), tubulin (green), and Aurora B–tubulin PLA (red) was imaged using a spinning-disk confocal microscope. Z sections were stitched sequentially using Volocity 5.5 software to make a MOV file. Fig. 5 A represents a whole-cell projection of this video.


EB1 enables spindle microtubules to regulate centromeric recruitment of Aurora B

Budhaditya Banerjee, Cortney A. Kestner, and P. Todd Stukenberg

DOI: 10.1083/jcb.201307119
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