|
|
|
|
|
|
|
||
| ||||||||||||||||||||||||||
Index of Online Supplemental Material for
J. Cell Biol. 10.1083/jcb.200408172
Trajkovski et al.
• Figure S1 ICA512 is a substrate of µ-calpain cleavage both in vitro and within cells.
• Figure S2 Dynamin 2 (K44A)-GFP inhibits the uptake of transferring in INS-1 cells.
• Figure S3 GFP is not enriched in the nuclei of stimulated INS-1 cells.
• Figure S4 ICA512-HA3 is correctly processed and targeted to the nucleus of stimulated INS-1 cells.
• Figure S5 FRET images showing that ICA512-CFP does not interact with the control protein lsm4-YFP in the nucleus of stimulated INS-1 cells.
• Video 1 (236 K) Stack of serial optical confocal Z-sections showing the low levels of ICA512-GFP in the nuclei of resting INS-1 cells.
• Video 2 (376 K) Stack of serial optical confocal Z-sections showing the high levels of ICA512-GFP in the nuclei of stimulated INS-1 cells.
• Video 3 (276 K) Stack of serial optical confocal Z-sections showing the low levels of ICA512-HA3 in the nuclei of resting INS-1 cells.
• Video 4 (396 K) Stack of serial optical confocal Z-sections showing the high levels of ICA512-HA3 in the nuclei of stimulated INS-1 cells.
| ||||||||||||||||||||||||||
|
|
