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<div class="content_box"> | <div class="content_box"> | ||
− | <h1> | + | <h1>Improved Parts</h1> |
− | <h2> | + | <h2>BBa_K2443037 - T7 RNA Polymerase</h2> |
− | <p> | + | <p>Original part: BBa_I2032</p> |
+ | <p>Submitted by MIT in 2006 and designed by: Bartholomew Canton</p> | ||
+ | <p>Encodes only for the coding region of T7 RNA polymerase. In order to improve it and incorporate it into our Next<i>Vivo</i> we have codon optimized it and attached a 6 X His tag for easy purification. </P> | ||
Revision as of 05:44, 19 October 2017
Improved Parts
BBa_K2443037 - T7 RNA Polymerase
Original part: BBa_I2032
Submitted by MIT in 2006 and designed by: Bartholomew Canton
Encodes only for the coding region of T7 RNA polymerase. In order to improve it and incorporate it into our NextVivo we have codon optimized it and attached a 6 X His tag for easy purification.
Part BBa_K1791002
Part BBa_K17910012 contains two modules, a low efficiency ribosome binding site (RBS) expressing MS2 coat protein and a theophylline ribozyme with a MS2 aptamer at the 3’ end. To express MS2 coat protein the part utilizes expression of c-terminal 6x His tagged MS2 coat protein under a T7 promoter and a standard Shine Dalgarno sequence followed by a double terminator (BBa_0015). Downstream of the RBS is a T7 promoter followed by a theophylline ribozyme and a MS2 aptamer at the 3’ end. Coexpression of the two modules results in MS2 binding to the 3’ end of the theophylline ribozyme construct which allows for MS2-RNA purification by nickel affinity chromatography, RNA can then be eluted from the MS2-RNA complex by addition of theophylline.