Pankow, Sandra
Bamberger, Casimir http://orcid.org/0000-0002-3830-4486
Calzolari, Diego
Bamberger, Andreas
Yates, John R III http://orcid.org/0000-0001-5267-1672
Article History
First Online: 17 November 2016
Change Date: 30 November 2017
Change Type: Erratum
Change Details: In the version of this article initially published, Steps 11 and 20 mentioned an incorrect reagent. The correct text is: "Immediately add 1.5 ml of ice-cold TNI lysis buffer per 15-cm cell culture dish” (Step 11) and "Remove the supernatant, transfer the beads to a new tube and wash the beads three times with 20–100 bead volumes of TNI lysis buffer" (Step 20). The TNI lysis buffer was also not listed in the Materials. These errors have been corrected, and the following text was added to the Materials section: "TNI lysis bufferTNI lysis buffer is 0.5% Igepal CA-630, 50 mM Tris (pH 7.5), 250 mM NaCl, 1 mM EDTA, 1× Complete ULTRA EDTA-free Protease Inhibitor cocktail and 1× PhosStop." These errors, made during production, have been corrected in the HTML and PDF versions of the article.
Competing interests
: The authors declare no competing financial interests.