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. 2015 Nov 13;10(11):e0142606. doi: 10.1371/journal.pone.0142606

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© 2015 Shariq 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 3 — (A) Western blots showing co-immunoprecipitation (Co-IP) of Cagβ and CagE from cell extracts prepared from wild-type Hp (P12) and P12ΔcagE/cagE by anti-CagE and anti-Cagβ antibodies respectively. P12ΔcagE strain was used as a negative control. Antibodies used in the Western blots are marked. (B) Western blots showing Co-IP of CagV and CagE from cell extracts prepared from wild-type Hp (P12) and P12ΔcagE/cagE by anti-CagE and anti-CagV antibodies respectively. P12ΔcagE strain was used as a negative control. Antibodies used in the Western blots are marked. (C) Western blots showing GST-pull-down of CagV by GST-CagE. Antibodies used in Western blotting and precipitated proteins are indicated.