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pubmed-article:18998045pubmed:abstractTextThe capsid protein of PCV2 was expressed by using a recombinant baculovirus with insect Tn5 cells. A large amount of 28-kDa protein was released into the culture medium and self-assembled into PCV2-like particles (PCV2-LPs) with a buoyant density of 1.365 g/cm(3) and a diameter of 20 nm. PCV2-LPs were efficiently expressed, yielding 1 mg of purified particles per 10(7) Tn5 cells. The PCV2-LPs have antigenicity similar to that of authentic PCV2 particles, allowing us to develop a method for sensitively detecting PCV2-specific IgG antibodies. In addition, the PCV2-LPs appeared to be the most promising PCV2 vaccine candidate, by virtue of their potent immunogenicity.lld:pubmed
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pubmed-article:18998045pubmed:authorpubmed-author:TakedaNaokazu...lld:pubmed
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pubmed-article:18998045pubmed:year2008lld:pubmed
pubmed-article:18998045pubmed:articleTitleEfficient production of type 2 porcine circovirus-like particles by a recombinant baculovirus.lld:pubmed
pubmed-article:18998045pubmed:affiliationDepartment of Virology II, National Institute of Infectious Diseases, Gakuen 4-7-1, Musashi-murayama, Tokyo, 208-0011, Japan.lld:pubmed
pubmed-article:18998045pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:18998045pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed