Abstract
We demonstrate a simple scanless two-photon (2p) excited fluorescence microscope based on selective plane illumination microscopy (SPIM). Optical sectioning capability is presented and depth-resolved imaging of cameleon protein in C. elegans pharyngeal muscle is implemented.
Publication types
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Animals
-
Caenorhabditis elegans / metabolism
-
Coumarins / metabolism
-
Lighting / instrumentation*
-
Luminescent Proteins / metabolism
-
Microscopy, Fluorescence / instrumentation*
-
Muscles / metabolism
-
Pharynx / metabolism
-
Photons*
Substances
-
Coumarins
-
Luminescent Proteins
-
coumarin