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Int. J. Mol. Sci. 2012, 13(3), 3341-3353; doi:10.3390/ijms13033341

Generating Aptamers by Cell-SELEX for Applications in Molecular Medicine

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Received: 19 January 2012 / Revised: 1 February 2012 / Accepted: 1 March 2012 / Published: 12 March 2012
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Abstract: Aptamers are single-stranded oligonucleotides of DNA or RNA that bind to target molecules with high affinity and specificity. Typically, aptamers are generated by an iterative selection process, called systematic evolution of ligands by exponential enrichment (SELEX). Recent advancements in SELEX technology have extended aptamer selection from comparatively simple mixtures of purified proteins to whole living cells, and now cell-based SELEX (or cell-SELEX) can isolate aptamers that bind to specific target cells. Combined with nanotechnology, microchips, microfluidic devices, RNAi and other advanced technologies, cell-SELEX represents an integrated platform providing ultrasensitive and highly specific tools for clinical medicine. In this review, we describe the recent progress made in the application of cell-SELEX for diagnosis, therapy and biomarker discovery.
Keywords: aptamer; SELEX; molecular medicine aptamer; SELEX; molecular medicine
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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MDPI and ACS Style

Ye, M.; Hu, J.; Peng, M.; Liu, J.; Liu, J.; Liu, H.; Zhao, X.; Tan, W. Generating Aptamers by Cell-SELEX for Applications in Molecular Medicine. Int. J. Mol. Sci. 2012, 13, 3341-3353.

AMA Style

Ye M, Hu J, Peng M, Liu J, Liu J, Liu H, Zhao X, Tan W. Generating Aptamers by Cell-SELEX for Applications in Molecular Medicine. International Journal of Molecular Sciences. 2012; 13(3):3341-3353.

Chicago/Turabian Style

Ye, Mao; Hu, Jun; Peng, Minyuan; Liu, Jing; Liu, Jun; Liu, Huixia; Zhao, Xielan; Tan, Weihong. 2012. "Generating Aptamers by Cell-SELEX for Applications in Molecular Medicine." Int. J. Mol. Sci. 13, no. 3: 3341-3353.

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