RNA and DNA aptamers in cytomics analysis. Ulrich, H., Martins, A. H. B, & Pesquero, J. B. Cytometry. Part A : the journal of the International Society for Analytical Cytology, 59(2):220–31, June, 2004.
RNA and DNA aptamers in cytomics analysis. [link]Paper  doi  abstract   bibtex   
The systematic evolution of ligands by exponential enrichment (SELEX) technique is a combinatorial library approach in which DNA or RNA molecules (aptamers) are selected by their ability to bind their protein targets with high affinity and specificity, comparable to that of monoclonal antibodies. In contrast to antibodies conventionally selected in animals, aptamers are generated by an in vitro selection process, and can be directed against almost every target, including antigens like toxins or nonimmunogenic targets, against which conventional antibodies cannot be raised.
@article{Ulrich2004,
	title = {{RNA} and {DNA} aptamers in cytomics analysis.},
	volume = {59},
	issn = {1552-4922},
	url = {http://www.ncbi.nlm.nih.gov/pubmed/15170601},
	doi = {10.1002/cyto.a.20056},
	abstract = {The systematic evolution of ligands by exponential enrichment (SELEX) technique is a combinatorial library approach in which DNA or RNA molecules (aptamers) are selected by their ability to bind their protein targets with high affinity and specificity, comparable to that of monoclonal antibodies. In contrast to antibodies conventionally selected in animals, aptamers are generated by an in vitro selection process, and can be directed against almost every target, including antigens like toxins or nonimmunogenic targets, against which conventional antibodies cannot be raised.},
	number = {2},
	journal = {Cytometry. Part A : the journal of the International Society for Analytical Cytology},
	author = {Ulrich, Henning and Martins, Antonio Henrique B and Pesquero, João Bosco},
	month = jun,
	year = {2004},
	pmid = {15170601},
	keywords = {\#nosource, Animals, Binding, Combinatorial Chemistry Techniques, Combinatorial Chemistry Techniques: methods, Competitive, DNA, DNA: chemistry, Flow Cytometry, Flow Cytometry: methods, Humans, Ligands, Proteins, Proteins: analysis, Proteins: chemistry, Proteins: physiology, Proteomics, Proteomics: methods, RNA, RNA: chemistry},
	pages = {220--31},
}

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