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LNA-modified oligodeoxynucleotide hybridization with DNA microarrays printed on nanoporous membrane slides

MPG-Autoren

Liu,  Jian-Ping
Max Planck Society;

http://pubman.mpdl.mpg.de/cone/persons/resource/persons50180

Guerasimova,  Anna
Dept. of Vertebrate Genomics (Head: Hans Lehrach), Max Planck Institute for Molecular Genetics, Max Planck Society;

Schwartz,  Regine
Max Planck Society;

Lange,  Matthias
Max Planck Society;

Lehrach,  Hnas
Max Planck Society;

Nyarsik,  Lajos
Max Planck Society;

http://pubman.mpdl.mpg.de/cone/persons/resource/persons50363

Janitz,  Michal
Dept. of Vertebrate Genomics (Head: Hans Lehrach), Max Planck Institute for Molecular Genetics, Max Planck Society;

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Liu.pdf
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Zitation

Liu, J.-P., Guerasimova, A., Schwartz, R., Lange, M., Lehrach, H., Nyarsik, L., et al. (2006). LNA-modified oligodeoxynucleotide hybridization with DNA microarrays printed on nanoporous membrane slides. Combinatorial Chemistry & High Throughput Screening, 9(9), 591-597. doi:10.2174/138620706778249730.


Zitierlink: http://hdl.handle.net/11858/00-001M-0000-0010-83B9-6
Zusammenfassung
We report a robust method for the detection of hybridization events using a microarray-based assay on a nanoporous membrane platform. The technique is characterized by a hybridization time of only 1 hour and uses Cy5- labeled, 7-mer oligodeoxynucleotide probes modified with locked nucleic acid (LNA) nucleotides. We show that the volume of the DNA spotted onto a nanomembrane can be reduced to ∼4 nL with detectable signal intensity. Moreover, the amount of the DNA target could be reduced to 4 fmol. The described approach could dramatically increase the throughput of techniques based on sequencing by hybridization, such as oligofingerprinting, by decreasing the total number of probes that are needed for analysis of large clone sets and reduction of the sample/reagent consumption. The method is particularly advantageous when numerous hybridization-based assays must be performed for characterization of sample sets of 100,000 or more.