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    • 12. 发明授权
    • Cosmid vector for plant transformation and use thereof
    • 用于植物转化的粘粒载体及其用途
    • US08298819B2
    • 2012-10-30
    • US12306163
    • 2007-06-25
    • Yoshimitsu TakakuraToshihiko KomariYuji IshidaToshiyuki KomoriYukoh HieiToshiki MineTeruyuki Imayama
    • Yoshimitsu TakakuraToshihiko KomariYuji IshidaToshiyuki KomoriYukoh HieiToshiki MineTeruyuki Imayama
    • C12N15/82C12N15/19C12N15/00
    • C12N15/82C12N15/8205
    • The present invention aims to provide novel vectors for plant transformation.The vectors of the present invention are cosmid vectors having a full length of 15 kb or less characterized in that: 1) they contain an origin of replication of an IncP plasmid, but do not contain any origin of replication of other plasmid groups; 2) they contain the trfA1 gene of an IncP plasmid; 3) they contain an oriT of an IncP plasmid; 4) they contain the incC1 gene of an IncP plasmid; 5) they contain a cos site of lambda phage and the cos site is located outside the T-DNA; 6) they contain a drug resistance gene expressed in E. coli and a bacterium of the genus Agrobacterium; 7) they contain a T-DNA right border sequence of a bacterium of the genus Agrobacterium; 8) they contain a T-DNA left border sequence of a bacterium of the genus Agrobacterium; 9) they contain a selectable marker gene for plant transformation located between 7) and 8) and expressed in a plant; and 10) they contain restriction endonuclease recognition site(s) located between 7) and 8) for cloning a foreign gene.
    • 本发明旨在提供用于植物转化的新型载体。 本发明的载体是全长为15kb或更小的粘粒载体,其特征在于:1)它们含有IncP质粒的复制起点,但不含有其他质粒组的任何复制起点; 2)它们含有IncP质粒的trfA1基因; 3)它们含有一个IncP质粒的oriT; 4)它们含有IncP质粒的incC1基因; 5)它们含有λ噬菌体的cos位点,cos位点位于T-DNA外部; 6)它们含有在大肠杆菌中表达的耐药基因和农杆菌属的细菌; 7)它们含有农杆菌属细菌的T-DNA右侧序列; 8)它们含有农杆菌属细菌的T-DNA左边界序列; 9)它们含有位于7)和8之间的植物转化的选择性标记基因并在植物中表达; 和10)它们含有位于7)和8之间的限制性内切核酸酶识别位点,用于克隆外来基因。
    • 15. 发明授权
    • Method of transforming monocotyledons using scutella of immature embryos
    • 使用未成熟胚的小檗转化单子叶植物的方法
    • US07939328B1
    • 2011-05-10
    • US08428238
    • 1994-09-01
    • Hideaki SaitoYuji IshidaYukoh HieiToshihiko Komari
    • Hideaki SaitoYuji IshidaYukoh HieiToshihiko Komari
    • C12N15/82
    • C12N15/8205
    • Disclosed is a method of transforming monocotyledons which necessitates only a short period from the transformation to the regeneration of a whole plant as compared with the conventional methods, thus reducing the frequency of occurrence of mutants, and can be generally applied to the plants for which any system of regenerating the whole plants from protoplasts has not been established, and in which the material to be used can be readily prepared without any particular apparatuses. The present invention provides a method for transforming monocotyledons comprising transforming scutellum of an immature embryo of a monocotyledon with a bacterium belonging to genus Agrobacterium containing a desired gene, which immature embryo has not been subjected to a dedifferentiation treatment, to obtain a transformant.
    • 本发明公开了一种转化单子叶植物的方法,其与常规方法相比仅需要从整个植物的转化到再生的短的时间,从而降低突变体的发生频率,并且通常可以应用于任何 尚未建立从原生质体再生整株植物的系统,其中待使用的材料可以在没有任何特定装置的情况下容易地制备。 本发明提供一种用于将单子叶植物的未成熟胚的鳞片状细菌与含有未成熟胚的未分化处理的所需基因的农杆菌属的农杆菌属转化成单转基因的方法,得到转化体。