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    • 10. 发明授权
    • Plasmid vehicle for cloning in Agrobacterium tumefaciens
    • 用于在根癌土壤杆菌中克隆的质粒载体
    • US4605627A
    • 1986-08-12
    • US501959
    • 1983-06-07
    • Clarence KadoRobert C. TaitRonald C. Lundquist
    • Clarence KadoRobert C. TaitRonald C. Lundquist
    • C12N15/82C12N1/00C07H15/12C12N15/00
    • C12N15/8205
    • A cloning vector comprises a replication system derived from the pTAR plasmid and capable of stable maintenance in Agrobacterium tumefaciens. By combining the pTAR replication system with a second replication system from a host other than A. tumefaciens, shuttle vectors are obtained which allow manipulation in more than one host. The cloning vectors will usually include selectable markers having restriction enzyme sites which allow identification of recombinant molecules by insertional inactivation. By providing at least a fragment of the T-DNA region from the Ti plasmid, the subject vectors can be used to clone desired DNA fragments and transfer these fragments to the genome of a higher plant.The strain E. coli HB101/puc0400 was deposited on June 7, 1983 at the A.T.C.C. for patent purposes and granted accession no. 39377.
    • 克隆载体包含衍生自pTAR质粒并能够在根癌土壤杆菌中稳定维持的复制系统。 通过将pTAR复制系统与来自根瘤土壤杆菌以外的宿主的第二复制系统相结合,获得允许在多于一个宿主中操纵的穿梭载体。 克隆载体通常包括具有限制酶位点的选择标记,其允许通过插入失活来鉴定重组分子。 通过从Ti质粒提供至少一个T-DNA区的片段,可以使用目标载体来克隆所需的DNA片段并将这些片段转移到较高植物的基因组。 大肠杆菌HB101 / puc0400菌株于1983年6月7日在A.T.C.C. 专利用途并授予加入号。 39377。