Skip to main content
. 2019 May 22;8(5):487. doi: 10.3390/cells8050487

Figure 4.

Figure 4

Involvement of DRMs in the association of HCV core with HCV NS2 and the E1E2 complex. A4HAHCVcc-infected cells were lysed with Triton X-100 (Tx) buffer or Triton X-100 buffer + freezing (TxF) or Triton X-100 buffer + freezing + n-octyl-β-d-glucopyranoside buffer (TxnO). Core was quantified by a fully automated microparticle chemiluminescence immunoassay after immunoprecipitation (Ip) from cell lysates with (A) anti-HA, (B) anti-E2 (AR3A), anti-E1E2, (AR5A), (C) anti-E1 (A4) antibodies, and isotypic IgG. ns (not statistically significant), p > 0.05; * p < 0.05; ** p < 0.01.