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. 2016 Jan 4;16:1. doi: 10.1186/s12872-015-0179-x

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© Zhao et al. 2016

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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Fig. 2 — Effect of dealing with interleukin 2 (IL-2) on regulation of Scn3b in mouse myocardial HL-1 cells by quantitative real-time chain reaction (qRT-PCR) analysis. The mRNA samples were prepared from transfected HL-1 cells. Gapdh was used as a control for normalization. Scn3b was 3.73-fold up-regulated in transcription (p = 0.01). Each experiment was performed in triplicate presented as means and standard deviation (S.D.). *p < 0.05