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Samples of 25 ng of rIMPI proteins were loaded on a 12% (w/v) polyacrylamide Bis-Tris gel in reducing loading buffer. After incubation with anti-V5 as primary antibody and goat anti-mouse Ig conjugated to horseradish peroxidase as secondary antibody, rIMPI-1* revealed no signal, in contrast with rIMPI-1 and rIMPI-2.
