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

. 2021 Jan 21;12(1):105. doi: 10.1038/s41419-021-03411-6

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

© The Author(s) 2021

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

Fig. 5 — a Transcription factor binding sites of HOXB4. b–d Luciferase assays assessing the promoter of β-catenin. β-catenin promoter fragments were constructed, and luciferase activity relative to the control was measured in HOXB4-modified HeLa (b), C-33A (c), and SiHa (d) cells. e, f EMSA assay for the promoter of β-catenin. EMSA was used to detect the direct association of nuclear HOXB4 protein with its binding sites on the promoter regions of β-catenin in HOXB4-overexpressing HeLa (e) and C-33A (f) cells. g, h ChIP assays for the promoter of β-catenin. ChIP-qPCR assay in HOXB4-overexpressing HeLa (g) and C-33A (h) cells were performed with HOXB4 antibody and IgG antibody (negative control).