Open Access Article
This Open Access Article is licensed under a Creative Commons Attribution 3.0 Unported Licence
Correction: Nucleic acid detection with single-base specificity integrating isothermal amplification and light-up aptamer probes
Jaekyun
Baek
ac,
Jihyun
Park
b and
Youngeun
Kim
*abc
aInterdisciplinary Program in Bioengineering, Seoul National University, Seoul 08826, Republic of Korea. E-mail: youngeunkim@snu.ac.kr
bDepartment of Materials Science and Engineering, Seoul National University, Seoul, 08826, Republic of Korea
cResearch Institute of Advanced Materials, Seoul National University, Seoul, 08826, Republic of Korea
First published on 30th October 2024
Abstract
Correction for ‘Nucleic acid detection with single-base specificity integrating isothermal amplification and light-up aptamer probes’ by Jaekyun Baek et al., Nanoscale, 2024, https://doi.org/10.1039/D4NR01638F.
The original article contains an incorrect version of Fig. 1. The correct version of Fig. 1 is shown below.
 | ||
| Fig. 1 Schematic representation of CLASSIC. CLASSIC consists of three distinct reactions: amplification, digestion, and detection. Target DNA is exponentially amplified through recombinase polymerase amplification. Effectively, only the target DNA strand synthesized from the forward primer (green) that has pt modifications (black hexagon) remains intact after the enzymatic digestion. As a result, a pair of SDA probes (UHP and DHP) hybridizes to the single-stranded target and forms an aptameric core, leading to a dramatic enhancement in AO fluorescence. | ||
The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.
| This journal is © The Royal Society of Chemistry 2024 |