2010.igem.org/Team:Harvard/vectors/vectors
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- | <div>reporter series <a href="../ | + | <div>reporter series <a href="https://static.igem.org/mediawiki/2010/3/30/Reporter_Large.png" id="single_image" style="font-size:12px">click to enlarge</a></div><hr/> |
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- | <td style=""><p style="padding:10px | + | <td style="vertical-align:top"><p style="padding:10px"><br/>The reporter series vectors contain a reporter on the trailing end of the multiple cloning site such that expression of the reporter follows that of the inserted construct. We modified the vectors pORE R1 and pORE R3. pORE R1 contains the gusA reporter, and pORE R3 the smgfp reporter. </p></td> |
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Latest revision as of 20:15, 14 July 2010
meet the vectors
Our vectors are a modification of the pORE agrobacterium vector system developed by Coutu et al at Agriculture and Agrofood Canada. This vector system is designed for agrobacterium mediated plant transformation, and is a binary system with the vector containing the site for foreign constructs and the appropriate flanking regions to be recognized for introduction to the plant. The virulence genes are present on a separate vector contained in the agrobacterium, separate from the TDNA.
To modify the pORE series binary vectors to fit the biobrick standard, we digested the vectors with. We worked with two of each of the open, reporter, and expression series vectors, creating a total of six biobrick standard vectors suitable for agrobacterium mediated plant transformation.
open series click to enlarge |
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reporter series click to enlarge |
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expression series click to enlarge |
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