A Basic introduction to microscopy: Introduction Microscope configurations Transmitted light Fluorescence Fluorescence microscopes Stereoscopes Confocals Spinning disk confocals Two photon excitation TIRF Preparing your samples Objectives Images Deconvolution Image analysis Other points/FAQs |
Two photon excitation Two photon excitation can have advantages for imaging thicker samples. Rather than exciting the fluorophore with one photon, the excitation is produced by two lower energy photons. Only in a specific region is the excitation light focused with sufficient intensity to cause fluorescence.
Two photon excitation has a number of advantages:
A two photon excitation microscope doesn't need to use a pinhole. Because the sample is only excited in a very specific plane we know where the light has come from so all the light can be imaged and excellent z-axis resolution still be obtained.
The other big difference between our 2 photon and single photon systems is the laser used: 2 photon excitation requires a pulsed laser to enable excitation via the two step process (the half-way state is very short lived so the second photon needs to act very soon after the first). We have a femtosecond pulsed laser for doing this, and it cost a frightening amount of money. |