omation mbers - Society for Laboratory Automation and Screening
omation mbers - Society for Laboratory Automation and Screening
omation mbers - Society for Laboratory Automation and Screening
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TP023<br />
Katherine Dains<br />
Adeline Scientific<br />
Research<br />
1534 Plaza Lane, Suite 119<br />
Burlingame, Cali<strong>for</strong>nia 94010<br />
kdains@earthlink.net<br />
157<br />
Co-Author(s)<br />
Wensheng Chen<br />
In<strong>for</strong>mation <strong>and</strong> Data Management Software <strong>for</strong> Tracking Patient, Research, <strong>and</strong> Analysis<br />
Data in Small to Medium Clinical <strong>and</strong> Research Labs<br />
We have developed software <strong>for</strong> in<strong>for</strong>mation <strong>and</strong> data management <strong>for</strong> use in the small- to medium-sized life<br />
science research labs. The system is user configurable, uncomplicated, <strong>and</strong> af<strong>for</strong>dable. Most commercial data<br />
management software products available require sophisticated IT setup, in-house personnel or outside contractors<br />
to control <strong>and</strong> maintain the system. Our system will appeal to many laboratories that require flexibility <strong>and</strong><br />
specificity to their laboratory needs without the complexity <strong>and</strong> cost of a large <strong>and</strong> expensive product. At the<br />
center of the system is a configuration tool that can be set up to h<strong>and</strong>le various laboratory data management<br />
workflows such as recruitment <strong>and</strong> tracking of research study c<strong>and</strong>idates <strong>and</strong> related genetic studies. This<br />
intelligence tool is made possible through a proprietary data model cartridge technology. After completing the<br />
configuration process, the user can choose to deploy the data system or to merge data with existing systems. The<br />
system is designed with three-tier architecture in the <strong>for</strong>m of web applications thus allowing <strong>for</strong> easy upgrades <strong>and</strong><br />
remote access. Along with the simple web-based architecture, user-configurable data loading tools are provided<br />
that will adapt to most data importing tasks. In<strong>for</strong>mation can be entered <strong>and</strong> tracked over long periods of time,<br />
as well as easily retrieved through the web-based reporting structure. The system is built to support all major<br />
database products. We will present details on the architecture, detailed design specifications, <strong>and</strong> test results from<br />
collaborating research labs.<br />
TP024<br />
Juan Jose Diaz-Mochon<br />
University of Southampton<br />
Chemistry<br />
Highfield Campus<br />
Southampton SO17 1BJ United Kingdom<br />
jjd29@soton.ac.uk<br />
Novel PNA-Peptoid Conjugates as Antisense Drugs<br />
Co-Author(s)<br />
Laurent Bialy, Boon-ek Yingyongnarongkul,<br />
Adam Belson, Mark Bradley<br />
Peptide Nucleic Acid (PNA) has been developed in the last decade as a new DNA mimic which hybridises<br />
complementary DNA or RNA sequences with higher affinity than its counterparts. PNA presents a 2aminoethylglycine<br />
backbone instead of the DNA sugar-phosphonate moiety. This uncharged backbone allows<br />
PNA to display a stronger hybridisation with DNA or RNA <strong>and</strong> to be easily synthesised. These features prompted<br />
investigators to develop PNA analogues as promising c<strong>and</strong>idates <strong>for</strong> the antisense therapy strategies. Antisense<br />
drugs target genes that are active or over expressed in certain pathological processes thus disrupting the synthesis<br />
of disease-responsible proteins. However, the main drawback has been their lack of cellular permeability that<br />
has avoided their further development as efficient antisense drugs. A few promising PNA-conjugates have been<br />
reported but new models are necessary to improve cellular permeability <strong>and</strong> overall drug-like features. Herein a<br />
new type of PNA-conjugates with higher cellular permeability is introduced. These novel PNA oligomers are bound<br />
to peptoids that have been reported as successful transfection agents. A library of PNA analogues has been<br />
synthesised on solid phase using a novel deprotection strategy, <strong>and</strong> it has been tested on GFP-transfected cell<br />
cultures. Furthermore, this library will also be tested using a cell-based microchip assay.<br />
POSTER ABSTRACTS