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

. 2018 Feb 1;8:2134. doi: 10.1038/s41598-018-20571-2

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

© The Author(s) 2018

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

PMC Copyright notice

KP-10 increases BMP2 expression and Smad1/5/9 phosphorylation. (A and B) RT-PCR (upper panel) and real-time PCR (lower panel) were performed using total RNA isolated from cells treated with 5 or 50 μM KP-10 for 2 days (A) and 50 μM KP-10 for 1 and 2 days (B). *p < 0.05 and **p < 0.01 compared with the untreated control. Data represent the mean ± SEM of three individual experiments. (C) Cells were transfected with BMP2-luc (0.4 μg) for 6 h and then treated with KP-10 (5 or 50 μM). **p < 0.01 and ***p < 0.005 compared with the untreated control. Data represent the mean ± SEM of three individual experiments. (D) Cells were treated with 50 μM KP-10 for 4 days and harvested for Western blot analysis using the indicated antibodies. (E) C3H10T1/2 cells were treated with KP-10 for the indicated durations and harvested for Western blot analysis using the indicated antibodies.