Sökning: WFRF:(Schallmeiner Edith) > In vitro analysis o...
Fältnamn | Indikatorer | Metadata |
---|---|---|
000 | 03400naa a2200481 4500 | |
001 | oai:DiVA.org:uu-16648 | |
003 | SwePub | |
008 | 080602s2007 | |||||||||||000 ||eng| | |
024 | 7 | a https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-166482 URI |
024 | 7 | a https://doi.org/10.1073/pnas.06112291042 DOI |
040 | a (SwePub)uu | |
041 | a engb eng | |
042 | 9 SwePub | |
072 | 7 | a ref2 swepub-contenttype |
072 | 7 | a art2 swepub-publicationtype |
100 | 1 | a Gustafsdottir, Sigrun M.u Uppsala universitet,Institutionen för genetik och patologi4 aut |
245 | 1 0 | a In vitro analysis of DNA-protein interactions by proximity ligation |
264 | c 2007-02-27 | |
264 | 1 | b Proceedings of the National Academy of Sciences,c 2007 |
338 | a print2 rdacarrier | |
520 | a Protein-binding DNA sequence elements encode a variety of regulated functions of genomes. Information about such elements is currently in a state of rapid growth, but improved methods are required to characterize the sequence specificity of DNA-binding proteins. We have established an in vitro method for specific and sensitive solution-phase analysis of interactions between proteins and nucleic acids in nuclear extracts, based on the proximity ligation assay. The reagent consumption is very low, and the excellent sensitivity of the assay enables analysis of as few as 1-10 cells. We show that our results are highly reproducible, quantitative, and in good agreement with both EMSA and predictions obtained by using a motif finding software. This assay can be a valuable tool to characterize in-depth the sequence specificity of DNA-binding proteins and to evaluate effects of polymorphisms in known transcription factor binding sites. | |
653 | a DNA/*metabolism | |
653 | a DNA-Binding Proteins/*metabolism | |
653 | a Electrophoretic Mobility Shift Assay | |
653 | a Genetic Techniques | |
653 | a Models; Molecular | |
653 | a Molecular Probes/genetics/metabolism | |
653 | a Oligonucleotides/genetics/metabolism | |
653 | a Polymerase Chain Reaction | |
653 | a MEDICINE | |
653 | a MEDICIN | |
700 | 1 | a Schlingemann, Jörgu Uppsala universitet,Institutionen för genetik och patologi4 aut |
700 | 1 | a Rada-Iglesias, Alvarou Uppsala universitet,Institutionen för genetik och patologi4 aut |
700 | 1 | a Schallmeiner, Edithu Uppsala universitet,Institutionen för genetik och patologi4 aut0 (Swepub:uu)edsch087 |
700 | 1 | a Kamali-Moghaddam, Masoodu Uppsala universitet,Institutionen för genetik och patologi4 aut0 (Swepub:uu)masookam |
700 | 1 | a Wadelius, Claesu Uppsala universitet,Institutionen för genetik och patologi4 aut0 (Swepub:uu)claeswad |
700 | 1 | a Landegren, Ulfu Uppsala universitet,Institutionen för genetik och patologi4 aut0 (Swepub:uu)ulfland |
710 | 2 | a Uppsala universitetb Institutionen för genetik och patologi4 org |
773 | 0 | t Proceedings of the National Academy of Sciences of the United States of Americad : Proceedings of the National Academy of Sciencesg 104:9, s. 3067-3072q 104:9<3067-3072x 0027-8424x 1091-6490 |
856 | 4 | u http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Retrieve&list_uids=17360610&dopt=Citation |
856 | 4 | u http://www.pnas.org/content/104/9/3067.full.pdf |
856 | 4 8 | u https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-16648 |
856 | 4 8 | u https://doi.org/10.1073/pnas.0611229104 |
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