| Literature DB >> 23323290 |
Qiaole Zhao1, Ben Schelen, Raymond Schouten, Rein van den Oever, René Leenen, Harry van Kuijk, Inge Peters, Frank Polderdijk, Jan Bosiers, Marcel Raspe, Kees Jalink, Jan Geert Sander de Jong, Bert van Geest, Karel Stoop, Ian Ted Young.
Abstract
We have built an all-solid-state camera that is directly modulated at the pixel level for frequency-domain fluorescence lifetime imaging microscopy (FLIM) measurements. This novel camera eliminates the need for an image intensifier through the use of an application-specific charge coupled device design in a frequency-domain FLIM system. The first stage of evaluation for the camera has been carried out. Camera characteristics such as noise distribution, dark current influence, camera gain, sampling density, sensitivity, linearity of photometric response, and optical transfer function have been studied through experiments. We are able to do lifetime measurement using our modulated, electron-multiplied fluorescence lifetime imaging microscope (MEM-FLIM) camera for various objects, e.g., fluorescein solution, fixed green fluorescent protein (GFP) cells, and GFP-actin stained live cells. A detailed comparison of a conventional microchannel plate (MCP)-based FLIM system and the MEM-FLIM system is presented. The MEM-FLIM camera shows higher resolution and a better image quality. The MEM-FLIM camera provides a new opportunity for performing frequency-domain FLIM.Entities:
Mesh:
Year: 2012 PMID: 23323290 DOI: 10.1117/1.jbo.17.12.126020
Source DB: PubMed Journal: J Biomed Opt ISSN: 1083-3668 Impact factor: 3.170