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. 2017 May 18;7:2090. doi: 10.1038/s41598-017-02242-w

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© The Author(s) 2017

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/.

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Deletion analysis of the mSTING promoter in NIH3T3 and HEK293 cells. Schematic structures of the mSTING promoter reporter constructs were shown on the left. The numbering was relative to the transcription start site. Seven recombinant reporter plasmids and pGL-3 Basic were cotransfected with the pRL-TK into NIH3T3 and HEK293 cells, respectively. The levels of firefly luciferase activity were normalized to the Renilla luciferase activity. Each bar represented the mean ± SD of three independent experiments (n = 3, *p < 0.05 vs. pGL3-Basic).