Three-dimensional sub–100 nm resolution fluorescence microscopy of thick samples

被引：0

作者：

Manuel F Juette

Travis J Gould

Mark D Lessard

Michael J Mlodzianoski

Bhupendra S Nagpure

Brian T Bennett

Samuel T Hess

Joerg Bewersdorf

机构：

[1] Institute for Molecular Biophysics,Department of Biophysical Chemistry, and Department of New Materials and Biosystems

[2] The Jackson Laboratory,Department of Physics and Astronomy

[3] University of Heidelberg,undefined

[4] Max Planck Institute for Metals Research,undefined

[5] University of Maine,undefined

[6] Institute for Molecular Biophysics,undefined

[7] University of Maine,undefined

[8] Active Motif,undefined

[9] Inc.,undefined

来源：

Nature Methods | 2008年 / 5卷

关键词：

D O I：

暂无

中图分类号：

学科分类号：

摘要：

The ability to image thick volumes with invariant high axial and lateral resolution is a challenge for existing super-resolution fluorescence microscopy techniques. The combination of a double-plane detection scheme with fluorescence photoactivation microscopy (FPALM) allows three-dimensional sub-diffraction resolution imaging of samples as thick as whole cells.

引用

页码：527 / 529

页数：2

共 50 条

[1] Three-dimensional sub-100 nm resolution fluorescence microscopy of thick samples
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