Plant expression vector
A technology of expression vectors and vectors, applied in the field of plant expression vectors, can solve problems such as the inability to remove bacterial screening markers, and achieve the effects of ensuring biological safety, reducing costs, and simplifying operation steps
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Embodiment 1
[0039] Embodiment 1, preparation and identification of pWMB014 universal expression vector
[0040] Expression vectors pRTL2, pZP101, pZP201, pCAMBIA3301 and pBluescript II-KS(-) were purchased from Biovector Science Lab ( http: / / biovector.blog.163.com / ; Tel: 18901268599 ).
[0041] Cloning vector pEASY TM -T1 Simple was purchased from Beijing Quanshijin Biotechnology Co., Ltd., the product catalog number is CT111.
[0042]Expression vectors pAHC25 and pTCK303 have been disclosed in literature (Christensen et al., Plant Molecular Biology, 1992, 18: 675-689) and (Wang et al., Plant Molecular Biology Reporter, 2004, 22: 409-417), and the public can obtain them from China Agriculture Acquired from the Institute of Crop Science, Academy of Sciences.
[0043] SEQ ID NO: 1: a T-DNA region containing ubi promoter, before replacement; corresponding Figure 14 ;
[0044] SEQ ID NO: 2: multiple cloning site from pBluescript II-KS(-), corresponding to Figure 15 ;
[0045] SEQ ID...
Embodiment 2
[0065] Embodiment 2. The application of vector-the insertion and identification of GUS gene in pWMB014
[0066] C58C 1 Agrobacterium tumefaciens were purchased from Biovector Science Lab ( http: / / biovector.blog.163.com / ; Tel: 18901268599). The wheat variety Xinchun 9 is preserved by the National Crop Germplasm Bank and provided to users free of charge (Institute of Crop Science, Chinese Academy of Agricultural Sciences, Tel: 010-62189650).
[0067] 1. Insertion of GUS gene into pWMB014
[0068] Design a pair of PCR primers GUS014XbaI2F: 5′-AT TCTAGA ATGGTAGATCTGAGGGTAAATTTCT-3' and GUS014SacI2R:5'-AT GAGCTC TCACACGTGGTGGTGGTGGT-3′, amplify the 2050bp full-length sequence of the GUS gene from the pCAMBIA3301 vector, add XbaI and SacI restriction sites at both ends, and first connect the full-length sequence of the GUS gene to pEASY TM -T1 Simple cloning vector. Then, use XbaI and SacI respectively to pWMB014 vector and pEASY TM -T1 Simple recombinant cloning vector wa...
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