Qiuxinyuan12 (Talk | contribs) |
Qiuxinyuan12 (Talk | contribs) |
||
Line 423: | Line 423: | ||
<br/>DESCRIPTION</div></div> | <br/>DESCRIPTION</div></div> | ||
<div style="color:black;font-size:16px;font-size:18px;width:60%;"> | <div style="color:black;font-size:16px;font-size:18px;width:60%;"> | ||
− | <p align="justify">MicroRNAs, serve as critical gene expression regulators at the transcriptional and post-transcriptional levels, have also been found as important blood-based biomarkers for early detection of cancers. However, their current in vitro detection methods are relatively complex, costly and low sensitive. Our project attempts to establish a novel in vitro microRNA detection system which is rapid, efficient, sensitive and specific. In this system, CRISPR-Cas9 technique is modified to integrate with | + | <p align="justify">MicroRNAs, serve as critical gene expression regulators at the transcriptional and post-transcriptional levels, have also been found as important blood-based biomarkers for early detection of cancers. However, their current in vitro detection methods are relatively complex, costly and low sensitive. Our project attempts to establish a novel in vitro microRNA detection system which is rapid, efficient, sensitive and specific. In this system, CRISPR-Cas9 technique is modified to integrate with split-HRP reporting systems. The advanced rolling circle amplification technology and cell-free expression system are also involved and optimized. This system may ideally be compatible for the detection of various series of small non-coding RNAs. To our knowledge, we are the first to use the CRISPR-Cas9 system as a small non-coding RNA monitor in vitro. Its establishment and further development might provide a new approach for rapid and low-cost cancer screening, virus detection and curative efficacy assessment. </p></div> |
</div> | </div> | ||
<div class="row footer-link" style=""> | <div class="row footer-link" style=""> |
Revision as of 02:41, 12 October 2016