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Index of Online Supplemental Material for
J. Cell Biol. 10.1083/jcb.200712137
Goss et al.
• Figure S1 Post-Golgi vesicles in the cleavage furrow are distinct from satellite Golgi.
• Figure S2 SDCM analysis of YFP-GPI–labeled post-Golgi vesicles indicates trafficking into the cleavage furrow from both daughter cells.
• Figure S3 Quantitative imaging of VSVG-YFP in BSC1 cells by TIRFM differentiates between vesicles that leave the evanescent field and vesicles that fuse.
• Video 1 SDCM analysis reveals post-Golgi vesicles are directed to the cleavage furrow from both daughter cells.
• Video 2 Manual tracking of post-Golgi vesicles that are directed to the cleavage furrow from both daughter cells.
• Video 3 SDCM analysis of YFP-GPI–labeled post-Golgi vesicles indicates trafficking into the cleavage furrow from both daughter cells.
• Video 4 FRAP analysis suggests post-Golgi membrane accumulations in the cleavage furrow consist of individual vesicles.
• Video 5 TIRFM analysis reveals exocytosis of post-Golgi vesicles from both daughter cells at the cleavage furrow.
• Video 6 TIRFM analysis reveals exocytosis of post-Golgi vesicles from both daughter cells at the cleavage furrow.
• Video 7 TIRFM high resolution view of single exocytic vesicle that fuses at the cleavage furrow.
• Video 8 DIC time-lapse imaging indicates asymmetrical midbody inheritance in BSC1 cells.
• Video 9 DIC time-lapse imaging indicates asymmetrical midbody inheritance in Hela cells.
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