Abstract
Resolution in potential three-photon fluorescence scanning microscopy is discussed in terms of the three-dimensional optical transfer function. Images of layers and sharp edges are presented for a comparison of the resolution with that in two-photon fluorescence microscopic imaging. For the same fluorescence wavelength the resolution is almost the same in both cases. However, for a given illumination wavelength the resolution for imaging a thick object in the case of three-photon fluorescence imaging can be improved by as much as 40–50% relative to that in two-photon imaging.
© 1996 Optical Society of America
Full Article | PDF ArticleCorrections
Min Gu, "Resolution in three-photon fluorescence scanning microscopy: errata," Opt. Lett. 21, 1414-1414 (1996)https://www.osapublishing.org/ol/abstract.cfm?uri=ol-21-17-1414
OSA Recommended Articles
Min Gu and Damian Bird
J. Opt. Soc. Am. A 20(5) 941-947 (2003)
Keisuke Toda, Keisuke Isobe, Kana Namiki, Hiroyuki Kawano, Atsushi Miyawaki, and Katsumi Midorikawa
Biomed. Opt. Express 9(4) 1510-1519 (2018)
Régis Gauderon and Colin J. R. Sheppard
Appl. Opt. 38(16) 3562-3565 (1999)

