JoVE Journal
Biology
Biology
Esto contenido es Open Access.
Capítulos
Resumen
Please note that all translations are automatically generated.
A method is described to photoactivate single cells containing a caged fluorescent protein using two-photon absorption from a Ti:Sapphire femtosecond laser oscillator. To fate map the photoactivated cell, immunohistochemistry is used. This technique can be applied to any cell type.