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SWEHSC > Facility Cores > Cellular Imaging > About > Equipment & Services >

Deconvolution Microscope

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See also: Confocal Microscopy on the WWW, Fluorescence Techniques on the WWW
This page: Zeiss LSM510NLO-Meta, Fees, Advantages & Disadvantages, Instrument Capabilities, Menu

 

 


 

DeltaVision Restoration Microscopy System


  •  Location: Medical Research Building 330M (see map)
  •  Contact:
Dr. David Elliott, 626-7870
  •  Administration:
Dept. of Cell Biology & Anatomy

  • 
Fees for Services:
see below

Reminder: SWEHSC Investigators (including their staff and students) should contact the Cellular Imaging Core directly for training, assistance with planning experiments, instrument technical support, and assistance with analysis or the interpretation of results.

Fees:

Fees for Training: Users must complete a minimum of 6 hours of assisted use/training time before they will be allowed to use the instrument without assistance. Cost is currently $25/hr.

Fees for Use: Investigators will be charged a fee of $25/hour for time on the instrument (microscope use and/or computation are currently the same fee). Investigators that require the services of an instrument operator will be charged an additional fee of $15/hr.

Instrument Capabilities:


The DeltaVision Restoration Microscopy System (Applied Precision, Inc) includes a research-grade inverted Olympus IX 70 microscope (with a cooled CCD camera, fiber-optic coupled mercury arc lamp, high-speed filter changers, electronic shutters and a high precision x-y-z positioning system) that is coupled to a computer workstation running Linux and vendor-supplied software called SoftWorX. Automated multiple wavelength and/or time lapse imaging experiments can be performed on either fixed tissues or cultured cells (using the BiopTechs Delta-T Live Cell system).

Advantages & Disadvantages:

Advantages: high resolution fluorescence images, capable of 2D and 3D time-lapse, lower light intensity (compared to a confocal laser) means it is friendlier to live cells, has a greater dynamic range (4096 intensity levels) compared to older confocals, up to 5 probes per data set (limited to the available filter sets).

Disadvantages: Users must pay close attention to the many issues related to obtaining high-resolution images (e.g., correct coverslip thickness, refractive index of mounting media, how close the specimen is to the coverslip, etc), deconvolving a stack of images takes time (as image size and/or the number of images in a stack increases, so does processing time) which is billed at the above mentioned hourly rate.



Douglas W. Cromey, M.S.
Manager, SWEHSC Cellular Imaging Core

Office: AHSC 4212
Voice: 520-626-2824
FAX: 520-626-2097
Email: Cromey@Arizona.edu



Funded by NIEHS grant # ES06694

© 1996-2007, The University of Arizona
Last update:  May 9, 2007
Page Content:  Doug Cromey
Web Master:  Mike Kopplin