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. 2014 Jan 8;9(1):e85436. doi: 10.1371/journal.pone.0085436

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© 2014 Rose 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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(A) Immunoblot analysis of UCP2. Cell lysates from AD-N LCLs (N = 4) and AD-A LCLs (N = 6) were analyzed for UCP2 content. A total protein stain served as the loading control. The molecular weight of UCP2 was confirmed using molecular mass markers. (B) Quantitation of band densities demonstrates the significantly higher UCP2 content in AD-A LCLs as compared to AD-N LCLs. *p<0.01.