期刊
OPTICS LETTERS
卷 34, 期 6, 页码 836-838出版社
OPTICAL SOC AMER
DOI: 10.1364/OL.34.000836
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资金
- National Institutes of Health (NIH)
- National Science Foundation (NSF)
We report a scheme for 2D standing-wave total-internal-reflection fluorescence microscopy. Standing-wave patterns are generated by two interfering beams coupled through the objective lens. Period, angular orientation, and phase of standing waves are controlled entirely by acousto-optic deflectors. The lateral resolution improvement of 100 nm is combined with an axial selectivity of <100 nm. by utilizing an evanescent standing-wave pattern. This technique can provide real-time imaging of subresolution structures in live biological specimens near a glass-water interface. (C) 2009 Optical Society of America
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