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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WP052<br />
Jas Sanghera<br />
TTP LabTech<br />
Melbourn Science Park, Cambridge Road<br />
Royston SG8 6EE United Kingdom<br />
jas.sanghera@ttplabtech.com<br />
217<br />
Co-Author(s)<br />
David Pole<br />
Wayne Bowen<br />
A Homogenous Assay <strong>for</strong> Inhibition of Basal Proliferation in 96- <strong>and</strong> 384-Well Formats Using<br />
the Acumen Explorer<br />
Estimating <strong>for</strong> a given cell population, both proliferation <strong>and</strong> its rate is critical to experiments in a wide variety of<br />
disciplines <strong>for</strong> example, immunology, cardiovascular disease <strong>and</strong> cancer. For this reason, over the years a number<br />
of assays have been developed to measure these processes <strong>and</strong> the gold st<strong>and</strong>ard assay has remained the<br />
uptake of 3H Thymidine. Examples of other assays developed to obviate the use of 3H label are MTT Formazan<br />
(colorimetric), BrdU ELISA (fluorescence) <strong>and</strong> Acid Phosphatase (colorimetric). However, all these assays involve<br />
a number of steps. Using the Acumen Explorer laser scanning fluorescence microplate cytometer a simple<br />
homogenous quantitative assay can be per<strong>for</strong>med in both 96- <strong>and</strong> 384-well plate <strong>for</strong>mats. Experiments described<br />
here show how the Acumen Explorer can be used to follow the basal proliferation of both adherent <strong>and</strong> suspension<br />
cell lines <strong>and</strong> the effect of inhibitors Pacilitaxel <strong>and</strong> Anisomycin quantified.<br />
WP054<br />
Eric Schmidt<br />
Ahura Corporation<br />
46 Jonspin Road<br />
Wilmington, Massachusetts 01887<br />
eschmidt@ahuracorp.com<br />
Innovations in Photonics <strong>for</strong> Biotech Applications<br />
Co-Author(s)<br />
Daryoosh Vakhshoori<br />
Biotech researchers have had to adapt their techniques around the tools which have been available, often with<br />
high expense <strong>and</strong> sub-optimal results. Now, thanks to billions of dollars invested in telecommunications, new<br />
classes of instruments based on novel technologies are being directed at the problems confronting the biotech<br />
community. Semiconductor lightsources <strong>and</strong> MEMs offer high reliability, long life, <strong>and</strong> small packages with very<br />
high efficiency, making them an ideal replacement <strong>for</strong> traditional lasers <strong>and</strong> optics. With all these advantages,<br />
scientists <strong>and</strong> engineers are thinking “outside the box” combining cross disciplinary know-how to create new<br />
classes of instruments with advanced capabilities including: multiple wavelengths, modulation, scanning, <strong>and</strong> most<br />
of all portability. Breakthrough innovations come when incremental innovations converge on a new market. In the<br />
case of photonics, innovations underwritten by billions of dollars of telecom investment are bearing fruit in the<br />
medical, scientific <strong>and</strong> industrial field. Teams of physicists <strong>and</strong> engineers are working to develop low-cost mobile<br />
optical plat<strong>for</strong>ms which should revolutionize drug discovery by putting “Main Frame” power onto the researchers’<br />
desk top.These next generation systems will incorporate multiple semiconductor lightsources, the optics to<br />
manipulate the photons, the apparatus to expose the samples <strong>and</strong> the detectors to measure the results in “Lap<br />
Top” size instruments. The vision is to utilize the breakthroughs in semiconductor lasers <strong>and</strong> MEMs to provide<br />
maintenance free, reliable, high efficiency packages which offer more functionality than what is presently available.<br />
POSTER ABSTRACTS