Aim: To study the preparation and cleavage activity of Rz1198 directed against HPV-6bE1 and HPV-11E1 (HPV-6b/llE1) transcripts in vitro. Methods: HPV-6b/llE1 gene fragments were cloned into T-vector trader the control ofT7 promoter, ^32P-tabeled HPV-6b/I1E1 transcripts as target-RNAs were transcribed in vitro and purified by PAGE.
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