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. 2019 Mar 21;11(3):285. doi: 10.3390/v11030285

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© 2019 by the authors.

Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).

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Association of BSRF1 with other viral proteins. (A) HEK293T cells were cotransfected by lipofection with the indicated expression vectors. After 24 h, whole-cell lysates were prepared and a portion was subjected to immunoblotting using anti-FLAG and -HA antibodies. The remaining lysates were subjected to immunoprecipitation (IP) using an anti-FLAG antibody, followed by immunoblotting with anti-FLAG and -HA antibodies. (B) The lysates were immunoprecipitated with an anti-HA antibody, followed by immunoblotting. (C) HEK293 EBV-BAC (wild-type) cells were transfected by lipofection with the indicated vectors, and subjected to IP using an anti-FLAG antibody followed by immunoblotting.

Association of BSRF1 with other viral proteins. (A) HEK293T cells were cotransfected by lipofection with the indicated expression vectors. After 24 h, whole-cell lysates were prepared and a portion was subjected to immunoblotting using anti-FLAG and -HA antibodies. The remaining lysates were subjected to immunoprecipitation (IP) using an anti-FLAG antibody, followed by immunoblotting with anti-FLAG and -HA antibodies. (B) The lysates were immunoprecipitated with an anti-HA antibody, followed by immunoblotting. (C) HEK293 EBV-BAC (wild-type) cells were transfected by lipofection with the indicated vectors, and subjected to IP using an anti-FLAG antibody followed by immunoblotting.