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Two-colour two-photon confocal microscopy with isotropic three-dimensional resolution and parallel excitation

  • J. Ni
  • , L. Qiao
  • , C. Wang
  • , F. Zhao*
  • , Y. Cheng
  • , Z. Xu
  • *Corresponding author for this work
  • CAS - Shanghai Institute of Optics and Fine Mechanics
  • Sun Yat-Sen University

Research output: Contribution to journalArticlepeer-review

Abstract

We demonstrate a novel design of two-colour two-photon fluorescence microscope in which isotropic three-dimensional imaging resolution and high scanning speed can be achieved simultaneously. In our scheme, a three-dimensional optical lattice constructed by multi-beam interference is used for two-colour two-photon fluorescence excitation. Our simulation results show that a resolution of 113.5 nm can be achieved in both transverse and axial directions with two pump pulses at the wavelengths of 400 and 800 nm, respectively; meanwhile, imaging speed can be greatly improved compared with that of traditional two-photon scanning fluorescence microscopes.

Original languageEnglish
Pages (from-to)205-210
Number of pages6
JournalJournal of Microscopy
Volume234
Issue number2
DOIs
StatePublished - May 2009
Externally publishedYes

Keywords

  • Confocal microscopy
  • Three-dimensional isotropic resolution
  • Two-colour two-photon fluorescence excitation

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