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. 2015 Dec 23;15:1006. doi: 10.1186/s12885-015-2018-y

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© Hu et al. 2015

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. 1 — Expression of NETO2 in primary CRC tissues. a NETO2 mRNA expression in 57 paired human CRC and corresponding adjacent normal mucosa specimens were determined by real-time qPCR method. Gene expression results were normalized by internal control β-actin. (T, tumor tissues; N, adjacent normal tissues). b Protein expression levels of NETO2 in an independent set of 24 paired CRC and corresponding adjacent normal specimens were determined by Western blot analysis. β-actin was used as a loading control. The relative protein expression of NETO2 was quantified and normalized to β-actin. Each N was arbitrarily designated 1.0. (T: Tumor tissues; N: adjacent normal tissues, T vs N, p < 0.001)