TY - GEN
T1 - Optical sectioning using finite-sized, multiple aperture arrays in fluorescence direct-view microscopy; experimental results
AU - Smith, P. J.
AU - Taylor, C.
AU - McCabe, E. M.
PY - 1999
Y1 - 1999
N2 - Confocal fluorescence imaging is widely used, particularly for biological applications, and also notably in direct-view microscopes. Recent work has compared the use of coherent and incoherent illumination sources on the optical sectioning characteristics of fluorescence direct-view microscopes. However this detailed comparison has been done in theory. This paper addresses the experimental aspects of using coherent light sources in fluorescence imaging using a range of finite-sized, multiple-aperture arrays. The experimental difficulties of choosing a suitable uniform, flat, fluorescent plane with a high quantum efficiency are considered. Axial response curves obtained with a fluorescent laser dye sample are presented.
AB - Confocal fluorescence imaging is widely used, particularly for biological applications, and also notably in direct-view microscopes. Recent work has compared the use of coherent and incoherent illumination sources on the optical sectioning characteristics of fluorescence direct-view microscopes. However this detailed comparison has been done in theory. This paper addresses the experimental aspects of using coherent light sources in fluorescence imaging using a range of finite-sized, multiple-aperture arrays. The experimental difficulties of choosing a suitable uniform, flat, fluorescent plane with a high quantum efficiency are considered. Axial response curves obtained with a fluorescent laser dye sample are presented.
UR - https://www.scopus.com/pages/publications/0032684895
M3 - Conference contribution
AN - SCOPUS:0032684895
SN - 0819430757
T3 - Proceedings of SPIE - The International Society for Optical Engineering
SP - 236
EP - 240
BT - Proceedings of SPIE - The International Society for Optical Engineering
PB - Society of Photo-Optical Instrumentation Engineers
T2 - Proceedings of the 1999 Three-Dimensional and Multidimensional Microscopy: Image Acquisition and Processing VI
Y2 - 24 January 1999 through 25 January 1999
ER -