Comparison of actin speckle microscopy with phalloidin staining. Primary cultures of newt lung epithelial cells were microinjected with X-rhodamine actin. Time-lapse FSM was performed on a spinning ...

Localization of Alexa Fluor-594-α-factor-labeled endosomes (center; red in merge) and Abp140-3GFP (left; green in merge) in bni1-12 bnr1Δ cell. Abp140p binds F-actin and localizes to actin patches ...

Localization of Alexa Fluor-594-α-factor-labeled endosomes (red), Abp1-GFP- (green) and Abp140-3GFP- (green) labeled endocytic vesicles. It was possible to distinguish endocytic vesicles from actin c...

Localization of Alexa Fluor-594-α-factor-labeled endosomes (center; red in merge) and Abp140-3GFP (left; green in merge). Abp140p binds F-actin and localizes to actin patches and cables. Endosome mov...

Localization of Abp1-RFP (red; left) and Abp140-3GFP (green; center). By expressing Abp1-mRFP and Abp140–3GFP to visualize endocytic vesicles and actin cables respectively, we observed that approxim...

Four general zones of f-actin movement are seen in primary cultures of newt lung epithelial cells microinjected with X-rhodamine actin. At the leading edge and throughout the lamellipodium, f-actin s...

Localization of Alexa Fluor-594-α factor labeled endosomes (red; center) and Abp1-GFP labeled endocytic patches (green; left) in an arp3-D11A cell. Although the patches do not move off the plasma mem...

Chromophore-assisted laser inactivation (CALI) inactivates target proteins by generating reactive photoproducts such as reactive oxygen species (ROS) by intense irradiation of photosensitizer chromoph...

Chromophore-assisted laser inactivation (CALI) inactivates target proteins by generating reactive photoproducts such as reactive oxygen species (ROS) by intense irradiation of photosensitizer chromoph...

Chromophore-assisted laser inactivation (CALI) inactivates target proteins by generating reactive photoproducts such as reactive oxygen species (ROS) by intense irradiation of photosensitizer chromoph...