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Immunoprecipitation of NNV capsid protein with GHSC70 and GVDAC2. (A) The purified NNV and cell lysates from NNV-infected and noninfected GF-1 cells were used as input for IP. (B) Western blotting of proteins immunoprecipitated (IP) by rabbit antiserum against NNV capsid protein. (C) Western blotting of proteins immunoprecipitated by rabbit anti-GAPDH antibody, which was used as the negative control.
