Abstract
Axial resolution in conventional fluorescence microscopy is considerably worse than transverse resolution because the axial location of a specimen feature is not encoded directly in the image, but rather, is indicated by its degree of defocus.
© 1993 Optical Society of America
PDF ArticleMore Like This
Frederick Lanni, Vijay Krishnamurthi, and Brent Bailey
CThS1 Conference on Lasers and Electro-Optics (CLEO:S&I) 1995
Euiheon Chung, Daekeun Kim, and Peter T. C. So
TuI46 Biomedical Topical Meeting (BIOMED) 2006
A. Fragola and L. Aigouy
5143_139 European Conference on Biomedical Optics (ECBO) 2003