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. 2015 May 14;10(5):e0127239. doi: 10.1371/journal.pone.0127239

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© 2015 Kan 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 properly credited.

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Fig 5 — (A) Phosphorylated IKKα/β S176/180 and phosphorylated IκBα SS32/36 are also reduced in LTBP2-infected cells. Phosphorylated p65 serine 536 level is reduced in LTBP2-infected cells compared to VA in HONE1 and HK1. The p84 and α-tubulin were used as loading controls. (B) Matrigel plug tumors show a reduction in phosphorylated p65 S536 in LTBP2-transduced cells compared to VA. The p84 was used as loading control. (C) Subcellular fractionation results show that phosphorylated p65 S536 was reduced in the nuclear fraction of LTBP2-transduced cells compared to VA. The p84 was used as control to determine nuclear fraction, while α-tubulin was used as the control for the cytoplasmic fraction.