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. Author manuscript; available in PMC: 2013 Jul 15.
Published in final edited form as: Arch Biochem Biophys. 2012 Apr 30;523(2):181–190. doi: 10.1016/j.abb.2012.04.018

Fig. 7.

Fig. 7

(A) Immunoprecipitation of MEF cell lysate with anti-Pa28α, anti-Pa28γ, anti-Pa200 or anti-β1 antibodies causes co-immunoprecipitation of both 20S and 26S proteasome subunits, however while anti-β1 and anti-Pa200 pull out a comparable amount of S4, anti-Pa28α and anti-Pa28γ antibodies are relatively poor at co- immunoprecipitation of S4. Immunoprecipitation protocols were as reported in the legends to Figs. 3 and 4. Non-specific binding was measured through immunoprecipitation of anti-porin. (B) Depletion of S4 through immunoprecipitation causes a small loss of Pa28α and Pa28γ but a very large loss of Pa200. MEF cell lysates were subjected to three cycles of immunoprecipitation with either anti-S4 or anti-porin. Non-immunoprecipitated supernatants were then taken and run on Western blots.