Won Yung Choi, Ph.D. |
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To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Dear All, This upcoming webinar will be educational with very little commercial content (but will feature Zeiss LSM510 confocal system and Visiopharm's newCAST stereology software to illustrate the scientific principles of confocal stereology). Thank you. Won Yung Choi, Ph.D. Senior Product Scientist Visiopharm USA (New York City Office) 917-464-5633 Confocal Stereology: The Quantitative Approach to Immunofluorescence Please join us for a Webinar on February 22 Space is limited. Reserve your Webinar seat now at: https://www1.gotomeeting.com/register/365851585 By Dr. Won Yung Choi, Senior Products Scientist, Visiopharm Confocal laser scanning microscopy is widely used in biological sciences for improved optical resolution and contrast. This is obtained by illuminating the specimen with a focused scanning laser beam and by placing a pinhole aperture in the image plane in front of the electronic photon detector. Confocal images can also be produced by the use of spinning disks that perform tandem scans with multiple scanning beams. Both types of techniques result in rejection of signals from above and below the focal plane, producing clear, high-contrast images that are used for qualitative analysis of the specimen. Unfortunately, many researchers do not realize that it is possible - and desirable - to obtain an accurate, unbiased quantitative estimation on a confocal microscope setup. As a result, most scientists resort to either (1) a biased estimation by subjectively selecting fields of view from which to quantify (and spending too much time performing inaccurate quantification), or (2) producing visually pleasing images (which only demonstrate the qualitative aspects of their research questions). In this scientific presentation, a typical workflow using newCAST stereology software on a Zeiss LSM 510 confocal laser scanning microscope will be demonstrated for unbiased quantitative analysis on sampling fields that are correctly obtained using the principles of systematic uniform random sampling. Examples will include stereological estimation of (i) number of cells, (ii) length density of fibers, and (iii) volume of tissue. Title: Confocal Stereology: The Quantitative Approach to Immunofluorescence Date: Tuesday, February 22, 2011 Time: 9:00-10:00 AM Eastern Standard Time / 3:00 4:00 Central European Time After registering you will receive a confirmation email containing information about joining the Webinar. System Requirements PC-based attendees Required: Windows® 7, Vista, XP or 2003 Server Macintosh®-based attendees Required: Mac OS® X 10.4.11 (Tiger®) or newer Please let us know if you wish to unsubscribe to our webinar invitations. With kind regards, Lene Gerlach VP Business Development Visiopharm [hidden email] |
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