双光子激发显微术
荧光
荧光寿命成像显微镜
临床前影像学
化学
荧光显微镜
分子成像
光子
荧光团
生物物理学
显微镜
光学成像
光学
自体荧光
作者
Fan Feng,Heng Mao,Aimin Wang,Liangyi Chen
标识
DOI:10.1007/978-981-15-7627-0_3
摘要
Two-photon fluorescence imaging is a powerful tool for observing the dynamics of cells in vivo in intact tissue and is well suitable for imaging neuronal activity for neuroscience research. Due to the nonlinear two-photon absorption, the optical sectioning ability is inherent, resulting in two-photon images with high signal contrast and signal-to-noise ratio with efficient illumination. In addition, the longer wavelength excitation light in two-photon imaging compared to one-photon imaging suffers less scattering and absorption by tissue, which allows deeper penetration. Today, two-photon microscopy is being rapidly developed to adapt to various biological applications for high-speed, high-resolution, large-volume, long-term imaging in freely behaving animals.
科研通智能强力驱动
Strongly Powered by AbleSci AI