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. 2016 Dec 12;11(12):e0167449. doi: 10.1371/journal.pone.0167449

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© 2016 Zhang et al

This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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Fig 2 — (A) Representative images of western blotting analyses of KIF20A protein expression in eight matched pairs of cervical cancer tissue samples (T) and adjacent noncancerous tissues (ANT). α-Tubulin was used as the loading control. (B) The average T/ANT ratios of KIF20A mRNA expression in the paired cervical cancer (T) and adjacent noncancerous tissue sections (ANT) were quantified using qPCR and normalised against GAPDH. The error bars represent the standard deviation of the mean (SD), which was calculated from three parallel experiments. (C) Immunohistochemical staining of KIF20A protein in eight pairs of matched early-stage cervical squamous cell carcinoma tissues. *P < 0.05.