JP2012530947A5 - - Google Patents

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JP2012530947A5
JP2012530947A5 JP2012516561A JP2012516561A JP2012530947A5 JP 2012530947 A5 JP2012530947 A5 JP 2012530947A5 JP 2012516561 A JP2012516561 A JP 2012516561A JP 2012516561 A JP2012516561 A JP 2012516561A JP 2012530947 A5 JP2012530947 A5 JP 2012530947A5
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Japan
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microscope
counter
region
sample
phosphor
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JP2012516561A
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Japanese (ja)
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JP2012530947A (ja
JP5746161B2 (ja
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JP2012516561A 2009-06-26 2010-06-19 顕微鏡画像における蛍光の評価方法 Active JP5746161B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DE102009031231A DE102009031231A1 (de) 2009-06-26 2009-06-26 Verfahren und Anordnungen für die Fluoreszenzmikroskopie
DE102009031231.5 2009-06-26
PCT/EP2010/003705 WO2010149319A1 (de) 2009-06-26 2010-06-19 Verfahren zum auswerten von fluoreszenzereignissen in einem mikroskopbild

Publications (3)

Publication Number Publication Date
JP2012530947A JP2012530947A (ja) 2012-12-06
JP2012530947A5 true JP2012530947A5 (enExample) 2013-08-08
JP5746161B2 JP5746161B2 (ja) 2015-07-08

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JP2012516561A Active JP5746161B2 (ja) 2009-06-26 2010-06-19 顕微鏡画像における蛍光の評価方法

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US (1) US8988771B2 (enExample)
EP (1) EP2446314B1 (enExample)
JP (1) JP5746161B2 (enExample)
DE (1) DE102009031231A1 (enExample)
WO (1) WO2010149319A1 (enExample)

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DE102012216164B4 (de) * 2012-09-12 2016-04-28 Forschungsverbund Berlin E.V. Vorrichtung mit einer Anordnung optischer Elemente
JP6292238B2 (ja) * 2013-09-27 2018-03-14 株式会社ニコン 装置、システム、方法、及びプログラム
GB201318598D0 (en) * 2013-10-21 2013-12-04 Univ Leicester Improvements in or relating to super-resolution microscopy
DE102015016353A1 (de) 2015-12-16 2017-06-22 Horst Wochnowski PALM-Verfahren mit mehreren sich nur marginal voneinander unterscheidenden Fluorophoren
WO2019131947A1 (ja) * 2017-12-27 2019-07-04 国立研究開発法人理化学研究所 分光分析装置、分光分析方法、プログラム、記録媒体及び顕微鏡
CN111656246B (zh) * 2018-01-02 2022-07-29 伦敦大学国王学院 用于定位显微的方法和系统、计算机可读存储介质
US11674902B2 (en) * 2018-07-16 2023-06-13 Yissum Research Development Company Of The Hebrew University Of Jerusalem Ltd. System and method for use in fret microscopy
DE102018122816B9 (de) * 2018-09-18 2024-07-04 Carl Zeiss Meditec Ag Verfahren und Vorrichtung zum Bestimmen einer Eigenschaft eines Objekts
DE102018220779A1 (de) 2018-12-03 2020-06-04 Carl Zeiss Microscopy Gmbh Nachweisverfahren von induzierten Lichtsignalen in einer dreidimensionalen Region einer Probe
DE102019127775A1 (de) * 2019-10-15 2021-04-15 Carl Zeiss Microscopy Gmbh Lichtmikroskop und Verfahren zur Bildaufnahme mit einem Lichtmikroskop
EP4090951B1 (en) * 2020-01-16 2026-02-25 Yissum Research Development Company Of The Hebrew University Of Jerusalem Ltd System and method for use in fret microscopy
JP7565554B2 (ja) * 2020-05-22 2024-10-11 国立大学法人山梨大学 分光計、分析システム及び分析方法
DE102020006975A1 (de) * 2020-11-11 2022-05-12 Carl Zeiss Microscopy Gmbh Laser-Scanning-Mikroskop und Verfahren zum Justieren eines Laser-Scanning-Mikroskops
DE102020131047B4 (de) * 2020-11-24 2024-08-22 Abberior Instruments Gmbh Verfahren und Vorrichtung zur Aufnahme nanoskopischer Bilder mehrfach gefärbter Proben
AU2022234898A1 (en) 2021-03-12 2023-09-28 Stryker European Operations Limited Neurosurgical methods and systems for detecting and removing tumorous tissue

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WO2009115108A1 (en) * 2008-03-19 2009-09-24 Ruprecht-Karls-Universität Heidelberg A method and an apparatus for localization of single dye molecules in the fluorescent microscopy
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DE102008021641A1 (de) * 2008-04-30 2009-11-05 Carl Zeiss Microlmaging Gmbh Auflösungsgesteigerte Lumineszenzmikroskopie
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DE102008028490A1 (de) * 2008-06-16 2009-12-17 Carl Zeiss Microimaging Gmbh Beleuchtungsanordnung für die TIRF-Mikroskopie
DE102008049886B4 (de) 2008-09-30 2021-11-04 Carl Zeiss Microscopy Gmbh Vorrichtung, insbesondere ein Mikroskop, zur Untersuchung von Proben
DE102008054317A1 (de) 2008-11-03 2010-05-06 Carl Zeiss Microlmaging Gmbh Kombinationsmikroskopie
DE102008059328A1 (de) 2008-11-27 2010-06-02 Carl Zeiss Microimaging Gmbh Auflösungsgesteigerte Mikroskopie
US8693742B2 (en) * 2008-12-17 2014-04-08 The Regents Of The University Of Colorado Three-dimensional single-molecule fluorescence imaging beyond the diffraction limit using a double-helix point spread function

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