共 17 条
AXIAL RESOLUTION ENHACEMENT OF LIGHT-SHEET MICROSCOPY VIA TWO LIGHT-SHEETS
被引:0
作者:

Vannhu Le
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机构:
Le Quy Don Tech Univ, 236 Hoang Quoc Viet St, Hanoi, Vietnam Le Quy Don Tech Univ, 236 Hoang Quoc Viet St, Hanoi, Vietnam

Minhnghia Pham
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Le Quy Don Tech Univ, 236 Hoang Quoc Viet St, Hanoi, Vietnam Le Quy Don Tech Univ, 236 Hoang Quoc Viet St, Hanoi, Vietnam

Vandang Hoang
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Le Quy Don Tech Univ, 236 Hoang Quoc Viet St, Hanoi, Vietnam Le Quy Don Tech Univ, 236 Hoang Quoc Viet St, Hanoi, Vietnam
机构:
[1] Le Quy Don Tech Univ, 236 Hoang Quoc Viet St, Hanoi, Vietnam
来源:
APCCAS 2020: PROCEEDINGS OF THE 2020 IEEE ASIA PACIFIC CONFERENCE ON CIRCUITS AND SYSTEMS (APCCAS 2020)
|
2020年
关键词:
Light-sheet microscopy;
super-resolution;
fluorescence microscopy;
PLANE ILLUMINATION;
FLUORESCENCE MICROSCOPY;
STRUCTURED-ILLUMINATION;
CONTRAST;
D O I:
10.1109/apccas50809.2020.9301664
中图分类号:
TP18 [人工智能理论];
学科分类号:
081104 ;
0812 ;
0835 ;
1405 ;
摘要:
Light-sheet fluorescence microscopy has many advantages including high-speed, noninvasive and low photobleaching and photodamage. The light-sheet thickness of light-sheet microscopy is used to determine the axial resolution. However, the light-sheet thickness is limited by the light diffraction. In order to beyond this limit, inhere, we introduce a novel way based on the use of two light-sheets to achieve the enhancement of the axial resolution of light-sheet microscopy. Two images are captured by using both Gaussian light-sheet and negative light-sheet beams. From these two images, a new relationship between them is built to achieve the axial resolution image higher than the image of Gaussian light-sheet. Experimental result is performed, indicating that the effectiveness of the proposed method is better than traditional light-sheet microscopy.
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页码:236 / 239
页数:4
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European Mol Biol Lab, Cell Biol & Biophys Unit, D-69117 Heidelberg, Germany German Canc Res Ctr, Opt Nanoscopy Div, D-69120 Heidelberg, Germany

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German Canc Res Ctr, Opt Nanoscopy Div, D-69120 Heidelberg, Germany
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Engelhardt, Johann
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German Canc Res Ctr, Opt Nanoscopy Div, D-69120 Heidelberg, Germany
Bioquant, D-69120 Heidelberg, Germany German Canc Res Ctr, Opt Nanoscopy Div, D-69120 Heidelberg, Germany

Sahl, Steffen J.
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Max Planck Inst Biophys Chem, Dept NanoBiophoton, D-37077 Gottingen, Germany German Canc Res Ctr, Opt Nanoscopy Div, D-69120 Heidelberg, Germany

Hell, Stefan W.
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机构:
German Canc Res Ctr, Opt Nanoscopy Div, D-69120 Heidelberg, Germany
Bioquant, D-69120 Heidelberg, Germany
Max Planck Inst Biophys Chem, Dept NanoBiophoton, D-37077 Gottingen, Germany German Canc Res Ctr, Opt Nanoscopy Div, D-69120 Heidelberg, Germany

Hufnagel, Lars
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European Mol Biol Lab, Cell Biol & Biophys Unit, D-69117 Heidelberg, Germany German Canc Res Ctr, Opt Nanoscopy Div, D-69120 Heidelberg, Germany