Thermo Fisher Scientific Inc. announced a collaborative partnership with the newly opened Vascular Proteomics Group at the James Black Center, King's College London, headed by Dr. Manuel Mayr. Started in June 2007, the facility is equipped with the combination of a Thermo Scientific LTQ Orbitrap XL(TM) high performance mass spectrometer and the ETD-equipped Thermo Scientific LTQ XL(TM) system. The James Black Center is a research facility with a range of core competencies including genomics, proteomics, mulitphoton confocal microscopy and MRI.
"We are delighted that our new proteomics facility at the James Black Center will feature cutting- edge technology dedicated to cardiovascular research. Our primary focus will be on the ability of stem cells to affect cardiovascular repair," said Dr. Mayr.
http://www.bionity.com/news/e/77293/
A new resource that identifies regions of the human genome that regulate gene expression may help scientists learn about and develop treatments for a number of human diseases, according to researchers at Duke's Institute for Genome Sciences & Policy (IGSP).
"The majority of DNA in our bodies is packaged, or tightly structured," said Gregory Crawford, Ph.D., a researcher in the IGSP and one of the senior investigators on this study. "Our goal was to identify the areas of DNA across the entire genome that are not packaged, because we know those are the regions that are important in regulating gene activity."The researchers published their findings in the January 25, 2008 issue of the journal Cell. The study was funded by the Duke IGSP and the National Human Genome Research Institute.
They combined two known processes to look at regulatory regions across the whole human genome, Crawford said."We used an enzyme called DNase that has been known for decades to preferentially identify unpackaged regions of DNA," he said. "In this study, we identified all unpackaged regions within the entire genome using two extremely efficient methodologies: microarrays and sequencing."
Microarrays are glass slides on which scientists can simultaneously look at millions of short pieces of DNA. New sequencing technologies are able to determine the genetic code of millions of DNA fragments. Together, these tools generated guides to understanding the location of the unpackaged regions, and the researchers compared the results found using each method and found high levels of agreement.By combining the two methods, the researchers were able to scan the entire genome efficiently.
http://www.brightsurf.com/news/headlines/35531/Search_for_the_on_switches_may_reveal_genetic_role_in_development_and_disease.html
