Elaine Rasmussen |
You are invited to attend 2 live, interactive, web-based instructional seminars
sponsored by Photometrics, QImaging, MAG Biosystems & Media Cybernetics: ========================================================== 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 ========================================================== 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 ========================================================== Interested? Webinar Descriptions below... ========================================================== 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 ========================================================== 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. ========================================================== There is no charge to participate in these on-line seminars. Connection lines are limited, so reserve yours now. ========================================================== |
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