Abstract
We have developed a specific and sensitive nucleic acid amplification assay that is suitable for routine gene detection. The assay is based on a novel molecular genetic strategy in which two different RNA probes are hybridized to adjacent positions on a target nucleic acid and then ligated to form an amplifiable reporter RNA. The reporter RNA is then replicated up to a hundred billion-fold in a 30-min isothermal reaction that signals the presence of the target. The assay can detect fewer than 100 nucleic acid molecules; it provides quantitative results over a wide range of target concentrations and it employs a universal format that can detect any infectious agent.
Dates
Type | When |
---|---|
Created | 23 years ago (July 26, 2002, 10:43 a.m.) |
Deposited | 3 years, 4 months ago (April 13, 2022, 2 p.m.) |
Indexed | 1 month, 1 week ago (July 11, 2025, 6:46 a.m.) |
Issued | 29 years, 2 months ago (May 28, 1996) |
Published | 29 years, 2 months ago (May 28, 1996) |
Published Online | 29 years, 2 months ago (May 28, 1996) |
Published Print | 29 years, 2 months ago (May 28, 1996) |
@article{Tyagi_1996, title={Extremely sensitive, background-free gene detection using binary probes and beta replicase.}, volume={93}, ISSN={1091-6490}, url={http://dx.doi.org/10.1073/pnas.93.11.5395}, DOI={10.1073/pnas.93.11.5395}, number={11}, journal={Proceedings of the National Academy of Sciences}, publisher={Proceedings of the National Academy of Sciences}, author={Tyagi, S and Landegren, U and Tazi, M and Lizardi, P M and Kramer, F R}, year={1996}, month=may, pages={5395–5400} }