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. Author manuscript; available in PMC: 2012 Jun 1.
Published in final edited form as: J Virol Methods. 2011 Apr 13;174(1-2):99–109. doi: 10.1016/j.jviromet.2011.04.003

Fig. 4. Coomassie blue staining of rabbit and mouse anti-ebolavirus GP1,2 antibodies.

Fig. 4

Each of the polyclonal antibodies was purified from sera using the corresponding antigens conjugated to beads and monoclonal antibodies were purified from the supernatant of hybridoma cells grown in serum-free medium using protein A (for rabbit monoclonals) or protein G (for mouse monoclonals) beads. Two micrograms of each antibody were resolved on SDS-PAGE gel and stained.