期刊
JOURNAL OF BIOPHOTONICS
卷 3, 期 7, 页码 432-436出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/jbio.201000018
关键词
optics and photonics; cell biology; interference microscopy; fluorescence microscopy
资金
- Swiss National Science Foundation (SNSF) [205320-120118]
- CTI/KTI [9389.1]
- Swiss National Science Foundation (SNF) [205320-120118] Funding Source: Swiss National Science Foundation (SNF)
The authors have developed a live cell multimodality microscope combining epifluorescence with digital holographic microscopoy; it has been implemented with a de-coupling procedure allowing to separately measure from the quantitative phase important cell parameters including absolute volume, shape and integral intracellular retractive index. In combination with the numerouos different specific fluorescent cellular probes this multimodality microscopy can address important issues in cell biology. This is demosntrated by the study of intracellular calcium homeostasis associated with the change in cell volume, whihc play a critical role in the excitotoxicity induced neuronal death. [GRAPHICS] Comparison between quantitative phase (left) and fluorescence signal (right) on neuronal cellular bodies.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据