“…One microgram of Tag per lane was digested with trypsin (t) at a protease/protein mass ratio of 1:500 (lanes 2, 4, 6, 8, 10, 12, 14, 16, 18, and 20) and separated by 13.5% SDS-PAGE. Untreated Tag (u) (lanes 3,5,7,9,11,13,15,17,19, and 21) and 10-kDa marker proteins (m) (lane 1) were electrophoresed in parallel. Lanes 1-3 were Coomassie-stained, and lanes 4 -21 were analyzed by Western blotting with monoclonal antibodies whose epitopes in Tag are indicated in the schematic diagram.…”