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. 1999 Oct;73(10):8083–8094. doi: 10.1128/jvi.73.10.8083-8094.1999

FIG. 4.

FIG. 4

Coexpression of wild-type C-prM and NS2B-3181 components. Following infection with vTF7-3, BHK-21 cells were transfected with pTM3-C-prM alone (lane 3) or in combination with pTM3-NS2B (lane 4), pTM3-NS3181 (lane 5), pTM3-NS3181(S→A) (lane 6), pTM3-NS2B-3181 (lane 7), pTM3-NS2B plus pTM3-NS3181 (lane 8), or pTM3-NS2B plus pTM3-NS3181(S→A) (lane 9). Following immunoprecipitation with antiserum to prM (A) or a combination of antisera to NS2B and NS3 (B), proteins were separated by SDS–13% PAGE. Mock-infected cell lysate was immunoprecipitated in lane 1, and untransfected vTF7-3-infected cell lysate was immunoprecipitated in lane 2. The identities of the proteins are noted on the right side of each panel, and the positions of standards (in kilodaltons) are indicated on the left. A small amount of unprocessed NS2B-3181 can be seen in lane 7 of panel B. NS3181 has only a single internal methionine residue, while NS2B has four, contributing to the difference in band intensity.