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RECENT ADVANCES IN SUPER-RESOLUTION FLUORESCENCE MICROSCOPY BY FINCH HOLOGRAPHY

掲載日:
講演会

米国Johns Hopkins大のマイクロスコピーセンター長で医工学科教授のGary Brooker先生が、北見工大での国際会議のご出席の後、来る10月21日に、研究支援部ニコンイメージングセンター及び光細胞生理研究分野に見学に来られます。折角の機会ですので、Brooker先生にはご講演をいただくこととなりました。Brooker先生は新しい超解像顕微鏡の技術、特に、レーリーの2倍の解像限界を持つ「3D蛍光ホログラフィー顕微鏡」を開発されるとともに実際のバイオイメージングへの応用を推進されております。是非ともこの機会にご参加いただければ幸いです。

日時 10月21日(月)11:00–12:00
場所 電子科学研究所 1F会議室
Title RECENT ADVANCES IN SUPER-RESOLUTION FLUORESCENCE MICROSCOPY BY FINCH HOLOGRAPHY
Presenter Gary Brooker
Affiliation
  • Professor: Department of Biomedical Engineering, Johns Hopkins University, 9605 Medical Center Drive, Rockville, Maryland 20850 USA
  • Director: Microscopy Center, Johns Hopkins University Montgomery County Campus, Rockville, Maryland 20850 USA
Biology
1968 Ph.D. (Pharmacology) University of Southern California
1996–1998 Professor of Cell Biology, Department of Cell Biology, Georgetown University
1998–2007 Research Professor, Department of Biology, Johns Hopkins University
2007–2010 Research Professor, Department of Chemistry and Advanced Technology Laboratory, Whiting School of Engineering, Johns Hopkins University
2003– Director Microscopy Center, Montgomery County Campus, Johns Hopkins University
2011– Research Professor, Department of Biomedical Engineering, Whiting School of Engineering, Johns Hopkins University
Abstract

In this lecture I will chronicle progress over the last 6 years since the invention of Fresnel Incoherent Correlation Holography by Joseph Rosen and Gary Brooker. In its current state of development, picture perfect 3D images with resolution beyond the Rayleigh limit can be reconstructed from FINCH holograms acquired by fluorescence microscopy. A number of optical, electro-optical and computational advances by ours and other laboratories have made this possible. Those advances and new approaches from our group will be discussed and have enabled us to improve image resolution to about two times the Rayleigh limit in fluorescence microscopy. The simplicity of FINCH and the ability to use any fluorescent dye and microscope objective with varying magnification (10X-100X) and NA (0.4-1.4) make FINCH an attractive method for 3D super-resolution microscopy.

連絡先
北海道大学電子科学研究所
研究支援部ニコンイメージングセンター
特任助教 大友康平
TEL: 011-706-9442
e-mail address: otomo@es.hokudai.ac.jp
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