LabAutomation 2006 - SLAS
LabAutomation 2006 - SLAS
LabAutomation 2006 - SLAS
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<strong>LabAutomation</strong><strong>2006</strong><br />
12:00 pm Tuesday, January 24, <strong>2006</strong> Track 5: Frontiers Beyond BioPharma Room: Sierra/Ventura<br />
Wyndham Palm Springs Hotel<br />
Gary Gust<br />
Co-Author(s)<br />
Osmetech Molecular Diagnostics<br />
M. Reed<br />
Pasadena, California<br />
A. M. Aguinaldo<br />
gary.gust@osmetech.com<br />
L. Cheung<br />
Y. Liu<br />
J. Bumbarger<br />
D. Wurtz<br />
W.A. Coty<br />
Cystic Fibrosis Carrier Screening Test Performed Using a Microarray Platform Based<br />
on Electrochemical Detection of DNA Hybridization<br />
The eSensor ® DNA detection technology enables genotyping of multiple genetic disease markers using electrochemical detection of<br />
nucleic acid hybridization. Each eSensor cartridge contains an array of gold electrodes, each containing a sequence-specific capture<br />
probe covalently linked to the gold surface. Each target nucleic acid is bound to its appropriate electrode through sequence-specific<br />
hybridization to its capture probe, and then detected by hybridization of ferrocene-labeled signal probes and interrogation by alternating<br />
current voltammetry. Each gold electrode is coated with an insulating monolayer which minimizes non-specific binding and prevents<br />
signaling of unbound signal probes, eliminating the need for a wash step prior to detection. A cystic fibrosis (CF) carrier detection test<br />
has been developed for the eSensor system, providing multiplex amplification and detection of carriers for the 23 mutations of the CF<br />
transmembrane regulator gene recommended by the American College of Medical Genetics. Studies performed at external sites with 486<br />
samples demonstrated an overall concordance of individual mutation calls with DNA sequencing of 99.0%, with a miscall rate of 0.02%.<br />
3:00 pm Tuesday, January 24, <strong>2006</strong> Track 5: Frontiers Beyond BioPharma Room: Sierra/Ventura<br />
Wyndham Palm Springs Hotel<br />
Ryan Rodgers<br />
Co-Author(s)<br />
National High Magnetic Field Lab<br />
Geoffrey C. Klein, Florida State University<br />
Tallahassee, Florida<br />
Tanner M. Schaub, National High Magnetic Field Lab<br />
rodgers@magnet.fsu.edu<br />
Donald F. Smith, Florida State University<br />
Petroleomics: Mass Spectrometry Returns to Its Roots<br />
Sunghwan Kim, National High Magnetic Field Lab<br />
Jeremiah M. Purcell, Florida State University<br />
Christopher L. Hendrickson, National High Magnetic Field Lab<br />
Alan G. Marshall, Florida State University<br />
Ultrahigh-resolution Fourier Transform Ion Cyclotron Resonance Mass Spectrometry (FT-ICR MS) has recently spawned the new field<br />
of “Petroleomics”, specifically defined as the relationship between the chemical composition of petroleum derived material and its<br />
physical properties. The inherent high mass accuracy and high mass resolving power of FT-ICR MS provides the elemental composition<br />
assignment of thousands of different polar heteroatom containing species from a single crude oil. Until very recently, the FT-ICR analysis<br />
of complex, petroleum derived materials has been limited to polar heteroatom containing species amenable to ElectroSpray Ionization<br />
(ESI). Here we present the latest developments in FT-ICR mass spectral analysis of crude oils and asphaltenes along with the latest<br />
instrument developments that expand the analysis to include nonpolar, aromatic species found in crude oil. Included are initial results from<br />
a commercial Atmospheric Pressure PhotoIonization (APPI) source (nonpolar aromatic species) and recent results from ESI FT-ICR MS<br />
analysis of “heavy ends” (polar aromatic species). For a single oil sample, positive and negative mode ESI, as well as positive mode APPI<br />
FT-ICR results are presented. Automation of the data acquisition procedure is also discussed. All heteroatom containing (ESI and APPI) and<br />
PAH (APPI) classes are identified and their corresponding type and carbon number distributions presented. The level of detail provided by<br />
FT-ICR MS analysis is unrivaled and amazingly, complete analysis (polars, nonpolars, aromatics and semi-volatile compounds) consumes<br />
less than a drop of oil.<br />
Work supported by NSF CHE-99-09502, Florida State University, and the National High Magnetic Field Laboratory in Tallahassee, FL<br />
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