CONFOCALMICROSCOPY Archives

October 2014

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[log in to unmask][log in to unmask][log in to unmask], 6 Oct 2014 12:39:09 -0500472_windows-1252 *****
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*****

**Commercial Posting**

Leica Microsystems and BitesizeBio have organized three free web-
seminars in October that may be of interest to your lab staff or those you
know who are just taking up microscopic techniques: [...]54_6Oct201412:39:[log in to unmask][log in to unmask], 6 Oct 2014 15:52:06 -0400606_ISO-8859-1 *****
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Hi everyone,

we are looking for a camera (mounted on an Olympus microscope, BX-41) in
order to do some brightfield, histological, immunochemistry, imaging. At
least, 3.5 MPixels, budget 5-6K.

We are using the software Image Pro (Media Cybernetics) for running the
camera and analysis. We would like something compatible with that
sofware. [...]49_6Oct201415:52:[log in to unmask][log in to unmask], 6 Oct 2014 13:56:04 -0600532_UTF-8 *****
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Thorlabs sells a scientific camera with 4MP in that price range, at least
for the gigE version. I don't know anything about its compatibility with
Image Pro though.

Craig Brideau

On Mon, Oct 6, 2014 at 1:52 PM, Louis Villeneuve <
[log in to unmask]> wrote: [...]44_6Oct201413:56:[log in to unmask][log in to unmask], 6 Oct 2014 18:25:45 -0500743_ISO-8859-1 *****
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Dear fellow microscopists,

This is a reminder to SAVE THE DATE for this year’s Fall Symposium &amp; Business
Meeting, which will be held on November 20th, 2014 at the Whitehead Institute in
Cambridge, MA. For the first time in recent history, our Symposium will have a
theme – “Developing Microscopy Tools and Techniques.” The meeting will bring
developers of microscopy tools together with researchers interested in applying
said tools to their research. The keynote speaker [...]44_6Oct201418:25:[log in to unmask][log in to unmask], 7 Oct 2014 08:21:32 +0000755_us-ascii *****
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Dear microscopists

For the 7th time I will run my ImageJ/Fiji workshops 'introduction to ImageJ/Fiji' and 'macro writing in ImageJ' on Monday 15 and Tuesday 16 December 2014 in Leicester, UK. The workshops are a mixture of lectures and hands-on sessions. No prior knowledge of ImageJ, Fiji or macro ‘
Reply To:
Confocal Microscopy List <[log in to unmask]>
Date:
Wed, 8 Oct 2014 18:02:06 +0000
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Yes, indeed! Fantastic!

Dr Rosemary White
CSIRO Plant Industry
GPO Box 1600
Canberra, ACT 2601
Australia

T 61 2 6246 5475
F 61 2 6246 5334
________________________________________
From: Confocal Microscopy List [[log in to unmask]] on behalf of George McNamara [[log in to unmask]]
Sent: Wednesday, 8 October 2014 10:51 p.m.
To: [log in to unmask]
Subject: congratulations to Eric, Stefan and  W.E. for Nobel Prize in Chemistry, “ for the development of super-resolved fluores cence microscopy”

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congratulations to Eric, Stefan and W.E. for Nobel Prize in Chemistry

http://www.nobelprize.org/nobel_prizes/chemistry/laureates/2014/press.html


  Press Release

8 October 2014

The Royal Swedish Academy of Sciences
<http://www.nobelprize.org/redirect/links_out/prizeawarder.php?from=/nobel_prizes/chemistry/laureates/2014/press.html&object=kva&to=http://www.kva.se/en/>
has decided to award the Nobel Prize in Chemistry for 2014 to

*Eric Betzig*
Janelia Farm Research Campus, Howard Hughes Medical Institute, Ashburn,
VA, USA,

*Stefan W. Hell*
Max Planck Institute for Biophysical Chemistry, Göttingen, and German
Cancer Research Center, Heidelberg, Germany

and

*William E. Moerner*
Stanford University, Stanford, CA, USA

/“for the development of super-resolved fluorescence microscopy”/


    Surpassing the limitations of the light microscope

For a long time optical microscopy was held back by a presumed
limitation: that it would never obtain a better resolution than half the
wavelength of light. Helped by fluorescent molecules the Nobel Laureates
in Chemistry 2014 ingeniously circumvented this limitation. Their
ground-breaking work has brought optical microscopy into the nanodimension.

In what has become known as nanoscopy, scientists visualize the pathways
of individual molecules inside living cells. They can see how molecules
create synapses between nerve cells in the brain; they can track
proteins involved in Parkinson’s, Alzheimer’s and Huntington’s diseases
as they aggregate; they follow individual proteins in fertilized eggs as
these divide into embryos.

It was all but obvious that scientists should ever be able to study
living cells in the tiniest molecular detail. In 1873, the microscopist
Ernst Abbe stipulated a physical limit for the maximum resolution of
traditional optical microscopy: it could never become better than 0.2
micrometres. *Eric Betzig*, *Stefan W. Hell* and *William E. Moerner*
are awarded the Nobel Prize in Chemistry 2014 for having bypassed this
limit. Due to their achievements the optical microscope can now peer
into the nanoworld.

Two separate principles are rewarded. One enables the method /stimulated
emission depletion (STED) microscopy/, developed by Stefan Hell in 2000.
Two laser beams are utilized; one stimulates fluorescent molecules to
glow, another cancels out all fluorescence except for that in a
nanometre-sized volume. Scanning over the sample, nanometre for
nanometre, yields an image with a resolution better than Abbe’s
stipulated limit.

Eric Betzig and William Moerner, working separately, laid the foundation
for the second method, /single-molecule microscopy/. The method relies
upon the possibility to turn the fluorescence of individual molecules on
and off. Scientists image the same area multiple times, letting just a
few interspersed molecules glow each time. Superimposing these images
yields a dense super-image resolved at the nanolevel. In 2006 Eric
Betzig utilized this method for the first time.

Today, nanoscopy is used world-wide and new knowledge of greatest
benefit to mankind is produced on a daily basis.


//

My thanks to the Nobel committee for revealing what W.E. is.

--



George McNamara, Ph.D.
Single Cells Analyst
L.J.N. Cooper Lab
University of Texas M.D. Anderson Cancer Center
Houston, TX 77054
Tattletales http://works.bepress.com/gmcnamara/42

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