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. 2012 Jan;31(1):36–44. doi: 10.5732/cjc.011.10317

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Chinese Journal of Cancer

This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License, which allows readers to alter, transform, or build upon the article and then distribute the resulting work under the same or similar license to this one. The work must be attributed back to the original author and commercial use is not permitted without specific permission.

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Figure 3. — A-B, real-time quantitative PCR of BamHI-W (A) and EBER1, EBER2, EBNA1, EBNA2, LMP1, LMP2A, BARF1, BZLF1, and BRLF1 (B) in SUNE2 at different passages (P8, P10, P21, P38) and SUNE2 xenograft P1 (XUNE2-P1). B95-8 and C666 cells were used as positive controls. BamHI-W was detected with DNA template and the other genes were detected with cDNA templates by real-time quantitative PCR, and the housekeeping gene GAPDH was used as an internal control. C, Western blots showing EBNA1 and LMP1 expression in Raji, B95-8, C666, and SUNE2 cells. GAPDH was used as a loading control. Lysates from Raji, B95-8, and C666 cells were used as positive controls.