Neutrophil-specific rac2 knockout abolished the oscillation between the front and rear of active Rac in neutrophils.
The video shows the subcellular localization of Rac-FRET, of which the YFP/CFP fluorescence ratio indicates the location of active Rac in neutrophils of 3 dpf Tg(lyzC:Cas9, cry:GFP)pu26 zebrafish larvae injected with plasmids containing control or rac2 sgRNAs. Scale bar: 10 μm.
Yueyang Wang, Alan Y. Hsu, Eric M. Walton, Sung Jun Park, Ramizah Syahirah, Tianqi Wang, Wenqing Zhou, Chang Ding, Abby Pei Lemke, GuangJun Zhang, David M. Tobin, and Qing Deng
J Cell Sci
2021. 134:None-None; doi: 10.1242/jcs.258574