Analytical & Quantitative Light Microscopy Course

[Jennifer Waters]

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Analytical & Quantitative Light Microscopy Directors: Greenfield Sluder, University of Massachusetts Medical Center, Worcester and David Wolf, Sensor Technologies LLC Course Date: May 7 - 16, 2008 <a onclick="return top.js.OpenExtLink(window,event,this)" href="http://gosnold.mbl.edu/StudentApp/StudentApp.asp?CourseID=AQLM" target="_blank"> Online Application Form (<a onclick="return top.js.OpenExtLink(window,event,this)" href="http://www.mbl.edu/education/admissions/applications/pdf/aqlm.pdf" target="_blank"> PDF) Deadline: January 23, 2008 Student Course Evaluation 2007 Lecture Schedule (PDF format) <a onclick="return top.js.OpenExtLink(window,event,this)" href="http://www.mbl.edu/education/courses/special_topics/pdf/aqlm_wk1_07.pdf" target="_blank"> Week 1 | <a onclick="return top.js.OpenExtLink(window,event,this)" href="http://www.mbl.edu/education/courses/special_topics/pdf/aqlm_wk2_07.pdf" target="_blank">Week 2

A comprehensive and intensive course in light microscopy for researchers in biology, medicine, and material sciences. This course provides a systematic and in-depth examination of the theory of image formation and application of video and digital methods for exploring subtle interactions between light and the specimen. This course emphasizes the quantitative issues that are critical to the proper interpretation of images obtained with modern wide-field and confocal microscopes. This course is limited to 30 students.

Laboratory exercises, demonstrations, and discussions include: (1) geometrical and physical optics of microscope image formation including Abbe's theory of the microscope and Fourier optics; (2) interaction of light and matter; (3) phase contrast polarization and interference microscopy for the nondestructive analysis of molecular and fine-structural organization in living cells; (4) fluorescence microscopy, quantification of fluorescence, and GFP; (5) principles and application of digital video imaging, recording, analysis, and display; (6) digital image processing and quantitative digital image deconvolution; (7) ratiometric measurement of intracellular ion concentrations; (8) confocal microscopy; and (9) new advances in light microscopy such as FRET, FLIM, TIRF, and pattern illumination.

The program is designed primarily for: (1) university faculty, professional researchers, postdoctoral fellows, and advanced graduate students in the life sciences who wish to expand their experience in microscopy and to understand the quantitative issues associated with analysis of data obtained with optical microscopes; (2) individuals well-grounded in the physical sciences, who wish to exploit microscopy techniques for analyzing dynamic fine-structural and chemical changes; and (3) industrial scientists and engineers interested in advancing the design of equipment and techniques involving video and digital microscopy.

Lectures are followed by small group laboratory sessions and demonstrations. As a result, students will have opportunities for extensive hands-on experience with state-of-the-art optical, electronic, and digital imaging equipment guided by an experienced staff from universities and industry.

2007 Course Faculty & Lecturers:

Edward (Ted) Salmon, University of North Carolina, Chapel Hill

Richard Cardullo, University of California, Riverside

Rainer Heintzmann, Kings College London

Edward Hinchcliffe, University of Notre Dame

John Murray, University of Pennsylvania

Mary-Ann Mycek, University of Michigan

Champika Samarasekera, Sensor Technologies

Randi Silver, Weill Cornell Medical College

Aaron Straight, Stanford University

Jason Swedlow, University of Dundee

Jennifer Waters, Harvard Medical School

[vb-2]

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Dear All,

 

I would greatly appreciate any reference to the careful evaluation of the axial drift (thermal, ... etc.) during the photobleaching step in FRAP experiments (e.g. on a single-, 4- or 9-voxel resolution level of, let say ca. 80x80x450 nm per voxel). Fluorescent beads (Q-dots) and fluorescently labeled virus particles in a live or a fixed cell could be a nice system for the cross-validation of this very important test.  

 

Thank you very much in advance,

 

Vitaly

NCI-Frederick,

301-846-6575

 

 

 

[B. Prabhakar Pandian]

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http://listserv.acsu.buffalo.edu/cgi-bin/wa?S1=confocal

Hello,
          We are looking for a vertical laminar flow hood of >4ft in
size. Although we have found some, none of them have a front sash which
we can close
when not in use. Can anyone let me know source where we can get one with
a fully closing front sash.

Thanks,

-Prabhakar

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B. Prabhakar Pandian
CFD Research Corporation
Biomedical Technology
215 Wynn Drive
Huntsville, AL 35805
Ph: 256-726-4942
Fax: [phone]