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. 2012 Apr 20;7(4):e35630. doi: 10.1371/journal.pone.0035630

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Summanen 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) 15 µg of rat brain extract was separated on a SDS-PAGE gel. PKCε was detected with anti-PKCε and HRP-conjugated goat anti-mouse antibodies. (B) Immunoprecipitations were performed with rat brain extract using a commercial anti-PKCε antibody (IgG Ab) and VHHs. PKCε (marked with an arrowhead) is visible at 90 kDa on lane 1. The bands at 55 kDa and 25 kDa on lane 1 represent the heavy and light chains of the anti-PKCε antibody. The bands at 16 kDa for A10, C1, D1, E6 and G8 represent the VHHs. A sample of uncoated protein A sepharose beads was included as a negative control (lane 2 = ctrl).