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- Mecklenburg, Michael, et al.
(författare)
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A Microarray platform for "omics" analysis
- 2001
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Ingår i: International Conference on Sensor Technology (ISTC 2001). - : SPIE. - 0277-786X. - 0819441198 - 9780819441195 ; 4414, s. 157-163
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Konferensbidrag (refereegranskat)abstract
- Microarray technology has revolutionized genetic analysis. However, limitations in genome analysis has lead to renewed interest in establishing 'omic' strategies. As we enter the post-genomic era, new microarray technologies are needed to address these new classes of 'omic' targets, such as proteins, as well as lipids and carbohydrates. We have developed a microarray platform that combines self- assembling monolayers with the biotin-streptavidin system to provide a robust, versatile immobilization scheme. A hydrophobic film is patterned on the surface creating an array of tension wells that eliminates evaporation effects thereby reducing the shear stress to which biomolecules are exposed to during immobilization. The streptavidin linker layer makes it possible to adapt and/or develop microarray based assays using virtually any class of biomolecules including: carbohydrates, peptides, antibodies, receptors, as well as them ore traditional DNA based arrays. Our microarray technology is designed to furnish seamless compatibility across the various 'omic' platforms by providing a common blueprint for fabricating and analyzing arrays. The prototype microarray uses a microscope slide footprint patterned with 2 by 96 flat wells. Data on the microarray platform will be presented.
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- Storgaard Sørensen, Claus, et al.
(författare)
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Chk1 regulates the S phase checkpoint by coupling the physiological turnover and ionizing radiation-induced accelerated proteolysis of Cdc25A.
- 2003
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Ingår i: Cancer Cell. - 1535-6108. ; 3:3, s. 247-58
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Tidskriftsartikel (refereegranskat)abstract
- Chk1 kinase coordinates cell cycle progression and preserves genome integrity. Here, we show that chemical or genetic ablation of human Chk1 triggered supraphysiological accumulation of the S phase-promoting Cdc25A phosphatase, prevented ionizing radiation (IR)-induced degradation of Cdc25A, and caused radioresistant DNA synthesis (RDS). The basal turnover of Cdc25A operating in unperturbed S phase required Chk1-dependent phosphorylation of serines 123, 178, 278, and 292. IR-induced acceleration of Cdc25A proteolysis correlated with increased phosphate incorporation into these residues generated by a combined action of Chk1 and Chk2 kinases. Finally, phosphorylation of Chk1 by ATM was required to fully accelerate the IR-induced degradation of Cdc25A. Our results provide evidence that the mammalian S phase checkpoint functions via amplification of physiologically operating, Chk1-dependent mechanisms.
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- Zhu, Bin, et al.
(författare)
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Innovative solid carbonate-ceria composite electrolyte fuel cells
- 2001
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Ingår i: Electrochemistry communications. - 1388-2481 .- 1873-1902. ; 3:10, s. 566-571
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Tidskriftsartikel (refereegranskat)abstract
- An innovative solid carbonate-oxide composite and related fuel cell (FC) technology is reported, It was discovered that solid carbonate-ceria composite (SCC) electrolytes were highly conductive with the material conductivity level varying from 0.001 to 0.2 S cm(-1) between 400 and 600 degreesC, and related FCs reached a power density between 200 and 600 mW cm(2) at a Current density of 300-1200 mA cm(-2) in the same temperature region. The SCCs were discovered to possess both oxide-ion (originating from the ceria phase) and proton (from the carbonate phase) conduction. Being an all-solid ceramic FC. the SCC can effectively reduce the material corrosion problem that is serious for the molten carbonate fuel cells (MCFCs). On the other hand, the innovative FC technology based on the SCC electrolytes developed in this work is similar to solid oxide fuel cells (SOF'Cs) and different from the MCFCs based on their ionic transport and FC processes, which facilitates a development of new type of advanced FC technology.
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