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. 2003 Jan;77(1):25–36. doi: 10.1128/JVI.77.1.25-36.2003

FIG. 3.

FIG. 3.

Analysis of TBEV-specific proteins by PAGE (A) and Western blotting (B). Infected PS cell monolayers were lysed 48 h postinfection for Sof and Za viruses and 72 h postinfection for Vs virus. Proteins were separated by electrophoresis on 7 to 15% polyacrylamide gels. For Western blotting, the proteins were transferred onto a nitrocellulose membrane and revealed by interaction with anti-TBEV antibodies. Lanes 1 and 5 contained mock-infected PS cells; the other lanes contained PS cells infected with Sof (lanes 2 and 6), Za (lanes 3 and 7), and Vs (lanes 4 and 9) viruses. Samples 1 to 4 were unheated and samples 5 to 8 were heated for 1 min at 95°C. The virus-encoded proteins and their masses are specified.