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SCIENTIFIC REPORT 2004 - Sylvester Comprehensive Cancer Center

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S H A R E D R E S O U R C E S<br />

S H A R E D R E S O U R C E S<br />

A N A L Y T I C A L I M A G I N G C O R E<br />

MANAGER<br />

Alberto Pugliese, M.D.<br />

Associate Professor of Medicine<br />

CO-MANAGER<br />

Beata R. Frydel, Ph.D.<br />

Associate Scientist of Neurosurgery<br />

PURPOSE<br />

Many research endeavors rely on state-of-theart<br />

imaging and molecular histology techniques<br />

requiring the use of complex and costly<br />

equipment not practical for the individual investigator<br />

to acquire and maintain. The Analytical<br />

Imaging Core is a campus-wide resource spearheaded<br />

by the Diabetes Research Institute and<br />

UM/<strong>Sylvester</strong>, with seed support from the dean<br />

of the University of Miami School of Medicine.<br />

The Juvenile Diabetes Research Foundation<br />

awarded additional support for a five-year period<br />

in December 2003. The core’s main goals are to:<br />

• Provide access to sophisticated, modern instrumentation<br />

for imaging and molecular analysis<br />

of tissue and cellular specimens to investigators.<br />

• Provide expertise, guidance, and training to<br />

core users and help them optimize protocols for<br />

their applications that can be shared with other<br />

investigators.<br />

SERVICES<br />

This core provides the following services:<br />

1) Confocal Microscopy: Confocal microscopy offers<br />

many advantages over standard fluorescent<br />

microscopy including increased sensitivity,<br />

resolution, and the ability to image relatively<br />

thick, fluorescently labeled biological specimens<br />

in two or three dimensions. Confocal<br />

microscopy creates an “optical section” of the<br />

cells or tissues being imaged and an increase in<br />

effective resolution due to a large increase in<br />

signal-to-noise ratio. As a result, outstanding<br />

images can be collected from cells and tissue<br />

sections that would otherwise yield little or no<br />

information.<br />

The workhorse instrument for confocal microscopy<br />

is the Zeiss LSM-510, which can detect<br />

up to five channels and four fluorescent<br />

channels simultaneously—from UV to far red,<br />

plus a separate detector for transmitted light.<br />

The outstanding beam control afforded by the<br />

Zeiss LSM-510 makes it an ideal instrument<br />

for other advanced fluorescent applications<br />

such as fluorescence resonance energy transfer<br />

(FRET), fluorescence recovery after photo<br />

bleaching (FRAP), or ratio-imaging for<br />

fluorescence quantitation. The core also is<br />

equipped with an Atto Instruments spinning<br />

disk confocal microscope (CARV), a confocal<br />

instrument particularly suited for live cell<br />

analysis, and video-rate (30 frames per second)<br />

imaging.<br />

2) Standard Epifluorescence Microscopy: The core<br />

also is equipped with a Leica DMIRB inverted<br />

microscope capable of performing triple fluorescence,<br />

phase contrast, and light microscopy, etc.<br />

UM/<strong>Sylvester</strong> <strong>Comprehensive</strong> <strong>Cancer</strong> <strong>Center</strong> Scientific Report <strong>2004</strong> 143

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