[FILM-Users 00363] COMMERCIAL Fwd: Fw: MSC webcast. Using microfluidics for real-time imaging of in vitro cell models
...forwarded for your information, related to the upcoming demonstration in FILM, Martin -------- Original Message -------- Subject: Fw: MSC webcast. Using microfluidics for real-time imaging of in vitro cell models Date: Tue, 28 May 2013 18:48:58 +0200 From: <donald.innes@merckgroup.com> To: Martin Spitaler <m.spitaler@imperial.ac.uk> *Donald Innes* CellASIC ONIX Specialist – UK & Ireland Merck Millipore, Bioscience Division Millipore UK Ltd * Mobile: +44 (0)7778 473 754*_ __donald.innes@merckgroup.com_ <mailto:donald.innes@merckgroup.com>_ __www.millipore.com_ <http://www.millipore.com/?cid=BIOS-S-ESIG-1052-1302-SP> Merck Millipore is a division of Merck KGaA, Darmstadt, Germany. CellASIC™ ONIX Microfluidic Platform <http://www.millipore.com/life_sciences/flx4/cellasic_live_cell_imaging?cid=BIOS-S-ESIG-1052-1302-SP> Text and link to Mandatory Information (in local language) Text and link to Mandatory Information (in English) ----- Forwarded by Donald Innes/MIUK/Merck on 28/05/2013 17:45 ----- Original message Nature Publishing Group continues its long standing tradition of providing the means for product manufacturers, service providers, publishers and other corporations to reach members of the scientific community who have opted-in to receive such messages. Nature Publishing Group does not endorse any of the products or services advertised here. To forward this email to a friend, please _click here_ <http://links.ealert.nature.com/servlet/FTFClickServlet?m=41609218&r=NTY2NjA2NTcyOTQS1&j=MTg5NTY0MjUxS0&mt=2&rj=MTg5NTIyMTkyS0&rt=1>. Custom webcast: sponsor retains sole responsibility for content *Using microfluidics for real-time imaging of /in vitro/ cell models** Date: Thursday May 30th 2013** Time: 8am PDT / 11am EDT 4pm BST / 5pm CEST Speakers: Dr Andrew Ball* EMD Millipore * Dr. KC Huang* Stanford University *_ Register for FREE_* <http://links.ealert.nature.com/ctt?kn=4&ms=NDE2MDkyMTgS1&r=NTY2NjA2NTcyOTQS1&b=0&j=MTg5NTY0MjUxS0&mt=2&rj=MTg5NTIyMTkyS0&rt=1> Cell cultures, by definition, inhabit the unsteady ground between tight, reproducible experimental control and the ability to simulate the complex and dynamic environments found /in vivo/. This webcast reveals how pioneering microfluidic technology enables the precise manipulation of physiologically relevant micro-environments, helping researchers connect cellular mechanisms with phenotypes and disease states. Microfluidic cell culture chambers allow crucial parameters such as media flow, temperature and gas environment to be automated. This enables researchers to recreate the mass transport environment of tissues, elicit cell responses to dynamic solution changes and enable long-term perfusion culture – a real-time, live cell analysis with unprecedented control. The first speaker, Dr. Andrew Ball, will review a specific workflow involving microfluidic chambers used with a fluorescent microscope and image analysis software, to provide insights for live cell dynamic applications such as host-pathogen interactions, cancer cell autophagy, and cell migration in a standardized format. Then, Dr. KC Huang, will discuss how specific microfluidic techniques have allowed him to study damped oscillations of bacterial growth in response to osmotic shock. Dr. Huang will describe the advantages of real-time, live cell analysis in a microfluidic context. 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                Martin Spitaler