| Literature DB >> 28625157 |
Tulsi Ram Damase1, Andrew D Ellington2, Peter B Allen1.
Abstract
Single-stranded DNA (ssDNA) oligonucleotides are useful as aptamers, hybridization probes and for emerging applications in DNA nanotechnology. Current methods to purify ssDNA require both a strand-separation step and a separate size-separation step but may still leave double-stranded DNA (dsDNA) impurities in the sample. Here, we use commercially available acrydite DNA primers to immobilize one strand of a PCR product within a polyacrylamide matrix. Electrophoresis moves the non-crosslinked DNA into the gel where the single-stranded product of desired size can be recovered. Our results show this method produces high yields of pure ssDNA.Entities:
Keywords: DNA; aptamer purification; single-strand generation
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Year: 2017 PMID: 28625157 PMCID: PMC6800053 DOI: 10.2144/000114557
Source DB: PubMed Journal: Biotechniques ISSN: 0736-6205 Impact factor: 1.993