Super-Resolution Imaging by Peyman Milanfar

Super-Resolution Imaging Peyman Milanfar ebook
Publisher: CRC Press
Format: pdf
ISBN: 1439819300, 9781439819302
Page: 492

The new microscopy technique, Live Structured-Illumination Microscopy Compare live SIM imaging to conventional fluorescence microscopy during two dynamic cellular processes. This was my first event of the conference, so I hope, dear readers, you will keep in mind that I was still getting my science head screwed back on as I took all this down… The session was chaired by U.V. Share11 / Share11 / 26 days ago / 26 days ago / 26 days ago / By Kym McNicholas 26 days ago / 26 days ago / By Andy Dunn 26 days ago / 25 days ago / 25 days ago / 25 days ago / 25 days ago / By Adam L. However, NAs more than the photoresist refractive index (~1.7) cause surface confinement of the image. A new twist on a sophisticated light microscopy technique is enabling researchers to capture short videos of fast-moving cellular processes while delivering super high resolution images of whole cells. A lot of application situation need to obtain high resolution video and image, such as astronomy, remote sensing, martial monitor and medical diagnosis (CT,MRI) etc. Alex Knight, Principal Research Scientist at the National Physical Laboratory is our first confirmed technology pitch at Nano4Life 2013. Our Image of the Month for October shows fluorescently labelled actin filaments imaged using super resolution microscopy. Presentations and discussions will focus on imaging cellular systems in 4D, novel tools and probes for imaging, super-resolution microscopy (SRM), and correlated light and electron microscopy. Microscopy is a central tool in both the nano- and life sciences. Higher resolution demands for semiconductor lithography may be fulfilled by higher numerical aperture (NA) systems. This whitepaper discusses the superresolution structured illumination method and how it is used to achieve three dimensional resolution enhancement through a combination of optics and image analysis. We used 3D-structured illumination microscopy (3D-SIM) to obtain subdiffraction ('super-resolution') images of plasmodesmata (PD) expressing a GFP-tagged viral movement protein (MP).