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A set of binary vectors were designed for a genomic gene (BDV1, Figure 3A) or CDS gene expression (BDV2, Figure 3B), gene silencing (BDV3, Figure 3C), and ethanol-inducible expression (BDV4, Figure 3D), respectively.
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The binary vector was designed for Agrobacterium tumefaciens to transfer the T-DNA into a plant cell nucleus (Joh and VanderGheynst, 2006).
The resulting binary vector was designated pXCGH.
N. benthamiana leaves were infiltrated with Agrobacterium tumefaciens strains containing pgR107 binary vectors that were designed to combine the advantages of A. tumefaciens-mediated transfection and viral infection.
Binary vectors were introduced into Agrobacterium strain EHA101 [46].
Binary vectors were transformed into Agrobacterium tumefacieriens strain gc101.
Binary vectors were transformed into Agrobacterium tumefaciens GV3850.
The binary vectors were transformed into Agrobacterium strain GV3101.
The resultant binary vectors were transformed into Agrobacterium stain AGL1.
The binary vector pCAMHSP was designed and mobilized into two Agrobacterium tumefaciens strains C58 and GV2260.
The binary vector was introduced into AglI by electrotransformation.
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