[FILM-Users 00441] Fwd: On Demand webcast: Real time imaging of cells with Super Resolution Microscopy.

[Martin Spitaler]

...forwarded for your information,

Martin



Begin forwarded message:

> *From:* Nature Publishing Group 
> <Nature.Publishing.Group at ealert.nature.com 
> <mailto:Nature.Publishing.Group at ealert.nature.com>>
> *Date:* 29 November 2013 10:03:37 GMT
> *To:* <t.magee at imperial.ac.uk <mailto:t.magee at imperial.ac.uk>>
> *Subject:* *On Demand webcast: Real time imaging of cells with Super 
> Resolution Microscopy.*
> *Reply-To:* <Nature.Publishing.Group at ealert.nature.com 
> <mailto:Nature.Publishing.Group at ealert.nature.com>>
>
> Macmillan Scientific Communication Webcast
> If you are unable to see the message below, click here to view 
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> nature.com webcasts 
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>
> Custom webcast: sponsor retains sole responsibility for content
>
> *The latest innovations
> **in real-time imaging of
> cells with Super
> Resolution Microscopy **
>
> A discussion into new technical innovations for
> Super Resolution Microscopy**
>
>
> Now available On Demand
> *
>
> 	
>
> **
> Speakers:
> *Dr Jennifer Lippincott-Schwartz*
> NIH Distinguished Investigator.
>
> *Dr Orla Hanrahan*
> Andor Technology.
>
> *Dr Susan Cox*
> King's College, London.
>
> *Register for FREE 
> <http://links.ealert.nature.com/ctt?kn=20&ms=NDQ0NjkyOTgS1&r=MTc3MDMyNTQyMwS2&b=0&j=MjE1Nzg1NTA5S0&mt=1&rt=0>*
>
> Due to the diffraction limit, standard light microscopes can at best 
> resolve features which are around 200nm apart, meaning that they are 
> unsuited to many biological applications. In this webcast, three 
> expert speakers will discuss super resolution microscopy, a rapidly 
> developing field that is breaking the diffraction limit to enable the 
> close examination of finely detailed biological samples.
>
> The current focus of the Super Resolution Microscopy community is to 
> increase the utility of existing localisation microscopy techniques 
> such as photo-activated localization microscopy (PALM) and stochastic 
> optical reconstruction microscopy (STORM) – in these methods, 
> fluorophores within a sample emit low levels of light, which is imaged 
> many thousands of times. This creates a single composite image with 
> resolution at the true molecular length scale. However, this process 
> is slow, meaning that these techniques are not best suited to 
> real-time imaging of cells and tissues.
>
> Our first speaker, Dr Jennifer Lippincott-Schwartz, will discuss 
> research currently underway using genetically-encoded photoactivatable 
> proteins (PA-FPs) for superresolution imaging which has dramatically 
> expanded the study of cellular organization, function and dynamics. 
> Our second speaker, Dr Susan Cox will go into some detail on the 
> algorithms which facilitate high resolution imaging of live cell 
> dynamics at the nanoscale and lastly Dr Orla Hanrahan will discuss 
> fast and sensitive detector technologies which are suitable for the 
> low light intensities of the single molecule techniques and the speed 
> required for live cell super resolution applications.
>
> *Register for FREE 
> <http://links.ealert.nature.com/ctt?kn=20&ms=NDQ0NjkyOTgS1&r=MTc3MDMyNTQyMwS2&b=0&j=MjE1Nzg1NTA5S0&mt=1&rt=0>
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