Figure - PMC

Skip to main content

An official website of the United States government

Here's how you know

Here's how you know

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

View full-text article in PMC

. 2020 Sep 30;12:9351–9362. doi: 10.2147/CMAR.S263222

Search in PMC
Search in PubMed
View in NLM Catalog
Add to search

© 2020 Chen et al.

This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).

PMC Copyright notice

CircCFL1 sponged miR-107. (A) Information on binding sites between CircCFL1 and miR-107. Prediction was performed by using the Starbase (http://starbase.sysu.edu.cn/) website. (B) Double luciferase reporter assay confirmed that CircCFL1 bound to miR-107. (C) MiR-107 expression after CircCFL1 overexpression and knockdown was detected through qPCR. (D) RNA pull-down assay confirmed the binding of CircCFL1 to miR-107. (CircCFL1 as a probe). (E) RNA pull-down assay confirmed the binding of CircCFL1 to miR-107 (miR-107 probe). **p < 0.01, ***p < 0.001.