CONFOCALMICROSCOPY Archives

September 2008

CONFOCALMICROSCOPY@LISTS.UMN.EDU

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Subject:
From:
Elaine Rasmussen <[log in to unmask]>
Reply To:
Confocal Microscopy List <[log in to unmask]>
Date:
Mon, 29 Sep 2008 14:44:13 -0500
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You are invited to attend 2 live, interactive, web-based instructional seminars 
sponsored by Photometrics, QImaging, MAG Biosystems & Media Cybernetics:

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Simultaneous IR-DIC and Fluorescence Imaging
Tuesday, September 30, 2008 at  10:00 AM  (Pacific Time)
Presenter Name: John Ossi, Regional Manager for QImaging Corporation 

For more information & to register, visit: 
http://www.magworldwide.com/education/webinar01220801.php

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Live Cell Fluorescence Imaging
Tuesday, September 30, 2008 at  11:30 AM  (Pacific Time)
Presenter Name: Nicholas Beavers, Applications Specialist with Media 
Cybernetics 
To register, visit 
For more information and to register, visit:
http://www.magworldwide.com/education/webinar07160801.php

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Interested?  Webinar Descriptions below...
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Simultaneous IR-DIC and Fluorescence Imaging

Microscopists performing microinjection studies often switch between 
fluorescence and Infra-red Differential Interference Contrast (IR-DIC) to 
visualize tissue and cellular structure in same field of view as fluorescence 
expression. This webcast showcases an innovative and inexpensive new 
software package that allows two cameras mounted on a microscope to each 
receive images from each mode of microscopy and to simultaneously image 
both image streams in a single overlaid frame. Images may be streamed to a 
live display and captured to disk.

Subjects include:
 
-	Setting up, aligning, and calibrating a dual-camera IR-DIC / 
Fluorescence system 
-	Assigning color look-up tables to each live image 
-	Overlaying images 
-	Capturing and presenting your data

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Live Cell Fluorescence Imaging

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 performed on the acquired image sets.  In this 
educational live webinar, attendees will learn how to optimally set up an 
automated and semi-automated microscope for performing protocols such as:

-	High speed fluorescence imaging 
-	Single-probe and multiple-probe fluorescence imaging 
-	3D time-lapse of single and multiple fluorescence probes 
-	Time-lapse imaging of cells in multi-well plates 
-	Ratiometric imaging 

Attendees will leave with a better understanding of the software and 
hardware options available for performance of live cell fluorescence imaging 
applications.

Bring your questions to these live, interactive web-based seminars.


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There is no charge to participate in these on-line seminars.  
Connection lines are limited, so reserve yours now. 
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