<?xml version="1.0" encoding="UTF-8" ?>
<rss version="2.0">
<channel>
  <title>MAG Webinar</title> 
  <description>Up-to-date MAG Webinar Schedule.</description>
   <link>http://magbiosystems.com/education/RSSfeed.xml</link> 
  <language>en-us</language> 
  <pubDate>Thu, 20 Dec 07 00:53:00 UT</pubDate> 
  <lastBuildDate>Thu, 20 Dec 07 00:53:00 UT</lastBuildDate> 
  <docs>http://www.magbiosystems.com/education/RSSfeed.xml</docs> 
  <generator>Marqui 4.9</generator> 
  <managingEditor>System Administrator</managingEditor> 
  <webMaster>webmaster@marqui.com</webMaster> 

<item>
<date>June 4, 2008</date>
<time>11:00 AM</time>
<title><![CDATA[Sieve Calibration and Particle Characterization Using Digital Image Analysis]]></title>
<description><![CDATA[<font id="tmpPasteIE">
<p><span class="hl"><span style="font-size: 10pt; font-family: arial;"><font color="#000000">Proper sieve calibration and accurate geometric measurements are essential requirements for anyone working with particles. Two common methods for particle characterization are sieving and image analysis. While image analysis is the preferred solution for</font></span></span></p></font>... 
]]></description>
<link>http://www.magbiosystems.com/education/webinar04230801.php</link>
</item>

<item>
<date>May 21, 2008</date>
<time>01:30 PM</time>
<title><![CDATA[Improved Stereoscopy Using Extended Depth-of-Field Processing]]></title>
<description><![CDATA[<font id=tmpPasteIE>
<p><font color=#000000><span style="font-size: 10pt; font-family: 'arial','sans-serif'">Stereomicroscopic observation of small organisms (such as drosophila and C. elegans), electronic circuits, and micro-machined components often requires the user to focus up and down through the z-axis to visualize the entire object. At each focus position</span></font></p></font>... 
]]></description>
<link>http://www.magbiosystems.com/education/webinar05210802.php</link>
</item>

<item>
<date>May 20, 2008</date>
<time>01:30 PM</time>
<title><![CDATA[Deconvolution of Confocal Fluorescence Microscopy Images]]></title>
<description><![CDATA[<div><span class=500341423-30082007><font face=Arial><font size=2><span class=890460613-04092007>Deconvolution&nbsp;has proven to be a powerful new&nbsp;tool for performing high-resolution multi-dimensional imaging of biological specimens.&nbsp; Used properly, deconvolution can&nbsp;dramatically increase the resolving capabilities and sensitivity of</span></font></font></span></div>... 
]]></description>
<link>http://www.magbiosystems.com/education/webinar05200801.php</link>
</item>

<item>
<date>May 19, 2008</date>
<time>01:30 PM</time>
<title><![CDATA[Deconvolution of Widefield Fluorescence Microscopy Images]]></title>
<description><![CDATA[<div><span class=500341423-30082007><font face=Arial><font size=2><span class=890460613-04092007>Deconvolution&nbsp;has proven to be a powerful new&nbsp;tool for performing high-resolution multi-dimensional imaging of biological specimens.&nbsp; It is used for increasing the sensitivity and improving the resolution of standard widefield microscopes</span></font></font></span></div>... 
]]></description>
<link>http://www.magbiosystems.com/education/webinar05190801.php</link>
</item>

<item>
<date>May 9, 2008</date>
<time>01:30 PM</time>
<title><![CDATA[Image Stitching of Large Specimens Using Automated Stages]]></title>
<description><![CDATA[<font id=tmpPasteIE><span class=000371320-26122007><font face=Arial size=2>Because the size of histology and pathology specimens generally exceed the field of view of the microscope, clinicians and researchers are often confronted with making a tradeoff between field-of-view (low magnification) and ability to resolve small image</font></span></font>... 
]]></description>
<link>http://www.magbiosystems.com/education/webinar05090801.php</link>
</item>

<item>
<date>May 6, 2008</date>
<time>01:30 PM</time>
<title><![CDATA[3D Reconstruction of Microscopy Images]]></title>
<description><![CDATA[<font size=+0> 
<div><span class=500341423-30082007><span class=890460613-04092007><font face=Arial size=2>Modern optical microscopy provides powerful tools for studying biological samples varying from sub-cellular structures to tissues. Transforming complex, multidimensional microscopy data sets into the actual presentation for use in lectures, web sites, or</font></span></span></div></font>... 
]]></description>
<link>http://www.magbiosystems.com/education/webinar05060801.php</link>
</item>

<item>
<date>May 1, 2008</date>
<time>01:30 PM</time>
<title><![CDATA[Counting, Sorting and Categorizing Objects in Images]]></title>
<description><![CDATA[<font id=tmpPasteIE><span class=421293301-24122007><font face=Arial><span class=009143214-24122007>Counting objects in images is a task that is routinely performed by scientists in a variety of disciplines.&nbsp;Researchers in&nbsp;material sciences and&nbsp;biology often share the goal of&nbsp;measuring the distribution of particles, cells, and other</span></font></span></font>... 
]]></description>
<link>http://www.magbiosystems.com/education/webinar05010801.php</link>
</item>

<item>
<date>April 30, 2008</date>
<time>01:30 PM</time>
<title><![CDATA[Live Cell Fluorescence Imaging]]></title>
<description><![CDATA[<font id=tmpPasteIE><font size=2> 
<p>Precise control and coordination of microscope optics, filters, stage, illumination, camera, incubator, pumps, and other devices is critical to the performance of any live cell study, particularly when quantitative analysis or deconvolution will be</p></font></font>... 
]]></description>
<link>http://www.magbiosystems.com/education/webinar04300801.php</link>
</item>

<item>
<date>April 22, 2008</date>
<time>01:30 PM</time>
<title><![CDATA[Simultaneous IR-DIC and Fluorescence Imaging]]></title>
<description><![CDATA[<font size=2> 
<div>Microscopists performing microinjection studies often switch between fluorescence and&nbsp;Infra-red Differential Interference&nbsp;Contrast (IR-DIC) to visualize tissue and cellular structure in same field of view as fluorescence expression.&nbsp;This</font></div>... 
]]></description>
<link>http://www.magbiosystems.com/education/webinar04220801.php</link>
</item>

<item>
<date>April 18, 2008</date>
<time>01:30 PM</time>
<title><![CDATA[Image Stitching of Large Specimens Using Automated Stages]]></title>
<description><![CDATA[<font id=tmpPasteIE><span class=000371320-26122007><font face=Arial size=2>Because the size of histology and pathology specimens generally exceed the field of view of the microscope, clinicians and researchers are often confronted with making a tradeoff between field-of-view (low magnification) and ability to resolve small image</font></span></font>... 
]]></description>
<link>http://www.magbiosystems.com/education/webinar04180801.php</link>
</item>

<item>
<date>April 16, 2008</date>
<time>01:30 PM</time>
<title><![CDATA[Tracking Objects in 2D and 3D]]></title>
<description><![CDATA[<font><span class=453520802-19122007><span class=828221316-19122007><span class=609574518-23122007><font face=Arial>Performing object&nbsp;<span class=531154618-23122007>tracking/</span>motility studies&nbsp;with the goal of statistically quantifying motion can be a daunting task.&nbsp; Living cells, for example, may cross the paths of other cells, make contact with other objects, move outside of the</font></span></span></span></font>... 
]]></description>
<link>http://www.magbiosystems.com/education/webinar04160801.php</link>
</item>

<item>
<date>April 9, 2008</date>
<time>01:30 PM</time>
<title><![CDATA[Counting, Sorting and Categorizing Objects in Images]]></title>
<description><![CDATA[<font id=tmpPasteIE><span class=421293301-24122007><font face=Arial><span class=009143214-24122007>Counting objects in images is a task that is routinely performed by scientists in a variety of disciplines.&nbsp;Researchers in&nbsp;material sciences and&nbsp;biology often share the goal of&nbsp;measuring the distribution of particles, cells, and other</span></font></span></font>... 
]]></description>
<link>http://www.magbiosystems.com/education/webinar04090801.php</link>
</item>

<item>
<date>April 7, 2008</date>
<time>01:30 PM</time>
<title><![CDATA[Managing, Mining, and Sharing Large Volumes of Images]]></title>
<description><![CDATA[Using Media Cybernetics' IQbase image database, our presenter will highlight and demonstrate the benefits of using a dedicated image database to store, manage and extract knowledge from your images.&nbsp; <br><br>If you&nbsp;spend time searching for images, wish... 
]]></description>
<link>http://www.magbiosystems.com/education/webinar04070801.php</link>
</item>

<item>
<date>March 20, 2008</date>
<time>10:00 AM</time>
<title><![CDATA[Intro to EFTEM (Energy-Filtered Transmission Electron Microscopy)]]></title>
<description><![CDATA[<font size=+0> 
<p><span style="font-family: 'arial','sans-serif'"><font size=3><font color=#000000><font id=tmpPasteIE><span style="font-size: 12pt; font-family: 'arial','sans-serif'"><font color=#000000>Energy-filtered transmission electron microscopy </font></span></font>(EFTEM) can reveal the elemental composition of natural and man-made structures at the micro-, nano-, and even sub-nanometer scale. This webinar is designed for microscope operators wishing to understand</font></font></span></p></font>... 
]]></description>
<link>http://www.magbiosystems.com/education/webinar03200802.php</link>
</item>

<item>
<date>March 20, 2008</date>
<time>01:30 PM</time>
<title><![CDATA[Counting, Sorting and Categorizing Objects in Images]]></title>
<description><![CDATA[<font id=tmpPasteIE><span class=421293301-24122007><font face=Arial><span class=009143214-24122007>Counting objects in images is a task that is routinely performed by scientists in a variety of disciplines.&nbsp;Researchers in&nbsp;material sciences and&nbsp;biology often share the goal of&nbsp;measuring the distribution of particles, cells, and other</span></font></span></font>... 
]]></description>
<link>http://www.magbiosystems.com/education/webinar03190801.php</link>
</item>

<item>
<date>March 18, 2008</date>
<time>01:30 PM</time>
<title><![CDATA[Deconvolution of Confocal Fluorescence Microscopy Images]]></title>
<description><![CDATA[<div><span class=500341423-30082007><font face=Arial><font size=2><span class=890460613-04092007>Deconvolution&nbsp;has proven to be a powerful new&nbsp;tool for performing high-resolution multi-dimensional imaging of biological specimens.&nbsp; Used properly, deconvolution can&nbsp;dramatically increase the resolving capabilities and sensitivity of</span></font></font></span></div>... 
]]></description>
<link>http://www.magbiosystems.com/education/webinar03180801.php</link>
</item>

<item>
<date>March 17, 2008</date>
<time>01:30 PM</time>
<title><![CDATA[Deconvolution of Widefield Fluorescence Microscopy Images]]></title>
<description><![CDATA[<div><span class=500341423-30082007><font face=Arial><font size=2><span class=890460613-04092007>Deconvolution&nbsp;has proven to be a powerful new&nbsp;tool for performing high-resolution multi-dimensional imaging of biological specimens.&nbsp; It is used for increasing the sensitivity and improving the resolution of standard widefield microscopes</span></font></font></span></div>... 
]]></description>
<link>http://www.magbiosystems.com/education/webinar03170801.php</link>
</item>

<item>
<date>March 14, 2008</date>
<time>01:30 PM</time>
<title><![CDATA[Live Cell Fluorescence Imaging]]></title>
<description><![CDATA[<font id=tmpPasteIE><font size=2> 
<p>Precise control and coordination of microscope optics, filters, stage, illumination, camera, incubator, pumps, and other devices is critical to the performance of any live cell study, particularly when quantitative analysis or deconvolution will be</p></font></font>... 
]]></description>
<link>http://www.magbiosystems.com/education/webinar03050801.php</link>
</item>

<item>
<date>March 12, 2008</date>
<time>01:30 PM</time>
<title><![CDATA[Fish Aging Using Image Analysis of Scales and Otoliths]]></title>
<description><![CDATA[<p><font><span class=453520802-19122007><span class=828221316-19122007><font face=Arial><font size=2>Measurement of annuli in fish scales and otoliths is a powerful method&nbsp;for aging individual fish and an effective way to collect data for tracking/logging trends among and between fish populations.&nbsp;</font></font></span></span></font></p>
<div><span class=453520802-19122007><span class=828221316-19122007><font id=tmpPasteIE><font face=Arial><font size=2><span class=828221316-19122007>Attendees will learn about the issues affecting</span></font></font></font></span></span></div>... 
]]></description>
<link>http://www.magbiosystems.com/education/webinar03120801.php</link>
</item>

<item>
<date>March 11, 2008</date>
<time>01:30 PM</time>
<title><![CDATA[Quantitative Image and Data Acquisition for Fluorescent Specimens -- Advice from a Facility Director]]></title>
<description><![CDATA[<font size=+0><font face=Arial><font size=2><span class=828221316-19122007> 
<div><span class=500341423-30082007><font face=Arial><font size=2>Attendees will learn about issues affecting the quantitative accuracy of&nbsp;<span class=890460613-04092007>fluorescence </span>images acquired through a microscope and will pick up tips and suggestions for&nbsp;<span class=890460613-04092007>improving image quality, making better use of the camera's light collection</span></font></font></span></div></span></font></font></font>... 
]]></description>
<link>http://www.magbiosystems.com/education/webinar01070801.php</link>
</item>

<item>
<date>March 10, 2008</date>
<time>01:30 PM</time>
<title><![CDATA[3D Reconstruction of Microscopy Images]]></title>
<description><![CDATA[<font size=+0> 
<div><span class=500341423-30082007><span class=890460613-04092007><font face=Arial size=2>Modern optical microscopy provides powerful tools for studying biological samples varying from sub-cellular structures to tissues. Transforming complex, multidimensional microscopy data sets into the actual presentation for use in lectures, web sites, or</font></span></span></div></font>... 
]]></description>
<link>http://www.magbiosystems.com/education/webinar03100801.php</link>
</item>

<item>
<date>March 7, 2008</date>
<time>01:30 PM</time>
<title><![CDATA[Image Stitching of Large Specimens Using Automated Stages]]></title>
<description><![CDATA[<font id=tmpPasteIE><span class=000371320-26122007><font face=Arial size=2>Because the size of histology and pathology specimens generally exceed the field of view of the microscope, clinicians and researchers are often confronted with making a tradeoff between field-of-view (low magnification) and ability to resolve small image</font></span></font>... 
]]></description>
<link>http://www.magbiosystems.com/education/webinar02280801.php</link>
</item>

<item>
<date>March 6, 2008</date>
<time>01:30 PM</time>
<title><![CDATA[Sieve Calibration and Particle Characterization Using Digital Image Analysis]]></title>
<description><![CDATA[<font id=tmpPasteIE> 
<p><span class=hl><span style="font-size: 10pt; font-family: arial"><font color=#000000>Proper sieve calibration and accurate geometric measurements are essential requirements for anyone working with particles. Two common methods for particle characterization are sieving and image analysis. While image analysis is the preferred solution for</font></span></p></span></font>... 
]]></description>
<link>http://www.magbiosystems.com/education/webinar03060801.php</link>
</item>

<item>
<date>February 26, 2008</date>
<time>01:30 PM</time>
<title><![CDATA[Counting, Sorting and Categorizing Objects in Images]]></title>
<description><![CDATA[<font id=tmpPasteIE><span class=421293301-24122007><font face=Arial><span class=009143214-24122007>Counting objects in images is a task that is routinely performed by scientists in a variety of disciplines.&nbsp;Researchers in&nbsp;material sciences and&nbsp;biology often share the goal of&nbsp;measuring the distribution of particles, cells, and other</span></font></span></font>... 
]]></description>
<link>http://www.magbiosystems.com/education/webinar02260801.php</link>
</item>

<item>
<date>February 25, 2008</date>
<time>01:30 PM</time>
<title><![CDATA[Tracking Objects in 2D and 3D]]></title>
<description><![CDATA[<font><span class=453520802-19122007><span class=828221316-19122007><span class=609574518-23122007><font face=Arial>Performing object&nbsp;<span class=531154618-23122007>tracking/</span>motility studies&nbsp;with the goal of statistically quantifying motion can be a daunting task.&nbsp; Living cells, for example, may cross the paths of other cells, make contact with other objects, move outside of the</font></span></span></span></font>... 
]]></description>
<link>http://www.magbiosystems.com/education/webinar02250801.php</link>
</item>

<item>
<date>February 15, 2008</date>
<time>01:30 PM</time>
<title><![CDATA[Performing FRAP Studies with a Widefield Microscope]]></title>
<description><![CDATA[<font id=tmpPasteIE><font face=Arial><span class=421293301-24122007><span class=915054118-24122007>Fluorescence Recovery After Photobleaching (FRAP) is a powerful </span>method&nbsp;for measuring global protein diffusion <span class=915054118-24122007>and has opened new areas of study in molecular and cell biology</span>.&nbsp;In this technique,<span class=915054118-24122007> molecules</span>&nbsp;of interest&nbsp;<span class=915054118-24122007>are </span>fluorescently</span></font></font>... 
]]></description>
<link>http://www.magbiosystems.com/education/webinar02150801.php</link>
</item>

<item>
<date>February 13, 2008</date>
<time>01:30 PM</time>
<title><![CDATA[Live Cell Fluorescence Imaging]]></title>
<description><![CDATA[<font id=tmpPasteIE><font size=2> 
<p>Precise control and coordination of microscope optics, filters, stage, illumination, camera, incubator, pumps, and other devices is critical to the performance of any live cell study, particularly when quantitative analysis or deconvolution will be</p></font></font>... 
]]></description>
<link>http://www.magbiosystems.com/education/webinar02130801.php</link>
</item>

<item>
<date>February 12, 2008</date>
<time>01:30 PM</time>
<title><![CDATA[Fish Aging Using Image Analysis of Scales and Otoliths]]></title>
<description><![CDATA[<p><font id=tmpPasteIE><span class=453520802-19122007><span class=828221316-19122007><font face=Arial><font size=2>Measurement of annuli in fish scales and otoliths is a powerful method&nbsp;for aging individual fish and an effective way to collect data for tracking/logging trends among and between fish populations.&nbsp;</font></font></span></span></font></p>
<div><span class=453520802-19122007><span class=828221316-19122007><font id=tmpPasteIE><font face=Arial><font size=2><span class=828221316-19122007>Attendees will learn about the issues affecting</span></font></font></font></span></span></div>... 
]]></description>
<link>http://www.magbiosystems.com/education/webinar02120802.php</link>
</item>

<item>
<date>February 7, 2008</date>
<time>01:30 PM</time>
<title><![CDATA[Managing, Mining, and Sharing Large Volumes of Images]]></title>
<description><![CDATA[Using Media Cybernetics' IQbase image database, our presenter will highlight and demonstrate the benefits of using a dedicated image database to store, manage and extract knowledge from your images.&nbsp; <br><br>If you&nbsp;spend time searching for images, wish... 
]]></description>
<link>http://www.magbiosystems.com/education/webinar02070802.php</link>
</item>

<item>
<date>January 31, 2008</date>
<time>01:30 PM</time>
<title><![CDATA[Performing FRAP Studies with a Widefield Microscope]]></title>
<description><![CDATA[<font id=tmpPasteIE><font face=Arial><span class=421293301-24122007><span class=915054118-24122007>Fluorescence Recovery After Photobleaching (FRAP) is a powerful </span>method&nbsp;for measuring global protein diffusion <span class=915054118-24122007>and has opened new areas of study in molecular and cell biology</span>.&nbsp;In this technique,<span class=915054118-24122007> molecules</span>&nbsp;of interest&nbsp;<span class=915054118-24122007>are </span>fluorescently</span></font></font>... 
]]></description>
<link>http://www.magbiosystems.com/education/webinar01310801.php</link>
</item>

<item>
<date>January 30, 2008</date>
<time>01:30 PM</time>
<title><![CDATA[3D Reconstruction of Microscopy Images]]></title>
<description><![CDATA[<font size=+0> 
<div><span class=500341423-30082007><span class=890460613-04092007><font face=Arial size=2>Modern optical microscopy provides powerful tools for studying biological samples varying from sub-cellular structures to tissues. Transforming complex, multidimensional microscopy data sets into the actual presentation for use in lectures, web sites, or</font></span></span></div></font>... 
]]></description>
<link>http://www.magbiosystems.com/education/webinar01300802.php</link>
</item>

<item>
<date>January 29, 2008</date>
<time>01:30 PM</time>
<title><![CDATA[Deconvolution of Confocal Fluorescence Microscopy Images]]></title>
<description><![CDATA[<div><span class=500341423-30082007><font face=Arial><font size=2><span class=890460613-04092007>Deconvolution&nbsp;has proven to be a powerful new&nbsp;tool for performing high-resolution multi-dimensional imaging of biological specimens.&nbsp; Used properly, deconvolution can&nbsp;dramatically increase the resolving capabilities and sensitivity of</span></font></font></span></div>... 
]]></description>
<link>http://www.magbiosystems.com/education/webinar01290801.php</link>
</item>

<item>
<date>January 28, 2008</date>
<time>01:30 PM</time>
<title><![CDATA[Deconvolution of Widefield Fluorescence Microscopy Images]]></title>
<description><![CDATA[<div><span class=500341423-30082007><font face=Arial><font size=2><span class=890460613-04092007>Deconvolution&nbsp;has proven to be a powerful new&nbsp;tool for performing high-resolution multi-dimensional imaging of biological specimens.&nbsp; It is used for increasing the sensitivity and improving the resolution of standard widefield microscopes</span></font></font></span></div>... 
]]></description>
<link>http://www.magbiosystems.com/education/webinar01280801.php</link>
</item>

<item>
<date>January 24, 2008</date>
<time>10:00 AM</time>
<title><![CDATA[Automated TEM Tomography Acquisition]]></title>
<description><![CDATA[<font id=tmpPasteIE>This live webinar is designed for microscope operators wishing to use tomography acquisition in DigitalMicrograph. &nbsp;The webinar will provide a detailed explanation of how to setup and launch an automated tilt series acquisition, along with techniques</font>... 
]]></description>
<link>http://www.magbiosystems.com/education/webinar01240802.php</link>
</item>

<item>
<date>January 23, 2008</date>
<time>01:30 PM</time>
<title><![CDATA[Counting, Sorting and Categorizing Objects in Images]]></title>
<description><![CDATA[<font id=tmpPasteIE><span class=421293301-24122007><font face=Arial><span class=009143214-24122007>Counting objects in images is a task that is routinely performed by scientists in a variety of disciplines.&nbsp;Researchers in&nbsp;material sciences and&nbsp;biology often share the goal of&nbsp;measuring the distribution of particles, cells, and other</span></font></span></font>... 
]]></description>
<link>http://www.magbiosystems.com/education/webinar01230801.php</link>
</item>

<item>
<date>January 22, 2008</date>
<time>01:30 PM</time>
<title><![CDATA[Simultaneous IR-DIC and Fluorescence Imaging]]></title>
<description><![CDATA[<font size=2> 
<div>Microscopists performing microinjection studies often switch between fluorescence and&nbsp;Infra-red Differential Interference&nbsp;Contrast (IR-DIC) to visualize tissue and cellular structure in same field of view as fluorescence expression.&nbsp;This</font></div>... 
]]></description>
<link>http://www.magbiosystems.com/education/webinar01220801.php</link>
</item>

<item>
<date>January 15, 2008</date>
<time>01:30 PM</time>
<title><![CDATA[Cell Viability Studies Using Image Analysis]]></title>
<description><![CDATA[<font id=tmpPasteIE><span class=421293301-24122007><font face=Arial>Identification and classification of&nbsp;mixed populations of&nbsp;cells into subgroups of healthy, stressed, apoptotic, and necrotic subpopulations can be readily performed using image processing techniques. Morphological differences and/or fluorescence</font></span></font>... 
]]></description>
<link>http://www.magbiosystems.com/education/webinar01150801.php</link>
</item>

<item>
<date>January 14, 2008</date>
<time>01:30 PM</time>
<title><![CDATA[Fish Aging Using Image Analysis of Scales and Otoliths]]></title>
<description><![CDATA[<p><font><span class=453520802-19122007><span class=828221316-19122007><font face=Arial><font size=2>Measurement of annuli in fish scales and otoliths is a powerful method&nbsp;for aging individual fish and an effective way to collect data for tracking/logging trends among and between fish populations.&nbsp;</font></font></span></span></font></p>
<div><span class=453520802-19122007><span class=828221316-19122007><font><font face=Arial><font size=2><span class=828221316-19122007>Attendees will learn about the issues affecting</span></font></font></font></span></span></div>... 
]]></description>
<link>http://www.magbiosystems.com/education/webinar01140801.php</link>
</item>

<item>
<date>January 11, 2008</date>
<time>01:30 PM</time>
<title><![CDATA[Tracking Objects in 2D and 3D]]></title>
<description><![CDATA[<font size=+0><span class=453520802-19122007><span class=828221316-19122007><span class=609574518-23122007><font face=Arial>Performing object&nbsp;<span class=531154618-23122007>tracking/</span>motility studies&nbsp;with the goal of statistically quantifying motion can be a daunting task.&nbsp; Living cells, for example, may cross the paths of other cells, make contact with other objects, move outside of the</font></span></span></span></font>... 
]]></description>
<link>http://www.magbiosystems.com/education/webinar01110801.php</link>
</item>

<item>
<date>January 9, 2008</date>
<time>01:30 PM</time>
<title><![CDATA[Live Cell Fluorescence Imaging]]></title>
<description><![CDATA[<font size="-0"><font size="2">
<p>Precise control and coordination of microscope optics, filters, stage, illumination, camera, incubator, pumps, and other devices is critical to the performance of any live cell study, particularly when quantitative analysis or deconvolution will be</p></font></font>... 
]]></description>
<link>http://www.magbiosystems.com/education/webinar01090801.php</link>
</item>

<item>
<date>January 7, 2008</date>
<time>01:30 PM</time>
<title><![CDATA[Quantitative Image and Data Acquisition for Fluorescent Specimens -- Advice from a Facility Director]]></title>
<description><![CDATA[<font size=+0><font size=+0><font size=+0>
<div><span class=500341423-30082007><font face=Arial><font size=2>Attendees will learn about issues affecting the quantitative accuracy of&nbsp;<span class=890460613-04092007>fluorescence </span>images acquired through a microscope and will pick up tips and suggestions for&nbsp;<span class=890460613-04092007>improving image quality, making better use of the camera's light collection</span></font></font></span></div></font></font></font>... 
]]></description>
<link>http://www.magbiosystems.com/education/webinar01070802.php</link>
</item>

</channel>
</rss>