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Volume 17 Issue 2
April 2002
    Citation: MA Yong ping, MENG Xiao—lin, XU Jin—ping. Amplification of Dendrolimus puctatus whenshanesis Cytovirus (DpCPV-W)in vitro in Sf21 Cell .VIROLOGICA SINICA, 2002, 17(2) : 137-141.
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    Amplification of Dendrolimus puctatus whenshanesis Cytovirus (DpCPV-W)in vitro in Sf21 Cell

    • 1.

      Institute of virology，Wuhan University．Wuhan 430072．China

    • Available online: 05 April 2002
    • We have studied amphificatlon of DpCPV W in vitro in Sf21 cell ln this paper．The results showed that DpCPV W could amplify is vitro in Sf2I ce t[and form normal potyhedra Acce~ional TeV eombinant enhancln in medium coutd synergist the infective rate of DpCPV—W in Sf21 cel1 in vitro． Bioassay indicated that the toxici’ty of DpCPV—W polyhedra amplified in Sf2 I cell was as violence a5 the polyhedra amplified in pine caterpillar By using the plaque purfieation technique in Sf21 cell，DpCPV— W could be purified n a single virion clone Ievd
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      Amplification of Dendrolimus puctatus whenshanesis Cytovirus (DpCPV-W)in vitro in Sf21 Cell

      • 1. Institute of virology，Wuhan University．Wuhan 430072．China

      Abstract: We have studied amphificatlon of DpCPV W in vitro in Sf21 cell ln this paper．The results showed that DpCPV W could amplify is vitro in Sf2I ce t[and form normal potyhedra Acce~ional TeV eombinant enhancln in medium coutd synergist the infective rate of DpCPV—W in Sf21 cel1 in vitro． Bioassay indicated that the toxici’ty of DpCPV—W polyhedra amplified in Sf2 I cell was as violence a5 the polyhedra amplified in pine caterpillar By using the plaque purfieation technique in Sf21 cell，DpCPV— W could be purified n a single virion clone Ievd

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