Synchronously pumped Raman laser for simultaneous degenerate and nondegenerate two-photon microscopy

  • Buttolph M
  • Mejooli M
  • Sidorenko P
  • et al.
6Citations
Citations of this article
20Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Two-photon fluorescence microscopy is a nonlinear imaging modality frequently used in deep-tissue imaging applications. A tunable-wavelength multicolor short-pulse source is usually required to excite fluorophores with a wide range of excitation wavelengths. This need is most typically met by solid-state lasers, which are bulky, expensive, and complicated systems. Here, we demonstrate a compact, robust fiber system that generates naturally synchronized femtosecond pulses at 1050 nm and 1200 nm by using a combination of gain-managed and Raman amplification. We image the brain of a mouse and view the blood vessels, neurons, and other cell-like structures using simultaneous degenerate and nondegenerate excitation.

Cite

CITATION STYLE

APA

Buttolph, M. L., Mejooli, M. A., Sidorenko, P., Eom, C.-Y., Schaffer, C. B., & Wise, F. W. (2021). Synchronously pumped Raman laser for simultaneous degenerate and nondegenerate two-photon microscopy. Biomedical Optics Express, 12(4), 2496. https://doi.org/10.1364/boe.421647

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free