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<p style="text-indent: 0px">Parts <b>BBa_K2605000 to BBa_K2605004 and BBa_K2605009</b> comprise the first iteration of a novel toolkit for targeted gene integration and maintenance of expression in eukaryotic chassis. The collection contains chromatin modifying elements that limit silencing of the integrated gene and minimize neighborhood effects. These elements, as well as the mCherry-BGH reporter gene with our improved CMV promoter, have restriction sites for directional cloning into part BBa_K2605002, which is a Multiple Cloning Site (MCS) flanked by distinct FRT (FLP recombinase recognition target) sites. The MCS carries sites for an arbitrary construct to be directionally cloned. </p> | <p style="text-indent: 0px">Parts <b>BBa_K2605000 to BBa_K2605004 and BBa_K2605009</b> comprise the first iteration of a novel toolkit for targeted gene integration and maintenance of expression in eukaryotic chassis. The collection contains chromatin modifying elements that limit silencing of the integrated gene and minimize neighborhood effects. These elements, as well as the mCherry-BGH reporter gene with our improved CMV promoter, have restriction sites for directional cloning into part BBa_K2605002, which is a Multiple Cloning Site (MCS) flanked by distinct FRT (FLP recombinase recognition target) sites. The MCS carries sites for an arbitrary construct to be directionally cloned. </p> | ||
<br> | <br> | ||
− | + | <p style="text-indent: 0px">In the first iteration of our gene integration strategy, | |
the FRT sites are leveraged for recombinase-mediated casette exchange (RMCE). | the FRT sites are leveraged for recombinase-mediated casette exchange (RMCE). | ||
Representing an experimental second design,<b>BBa_K2605006</b> is a prototype part intended to test our novel FLP-Beta strategy. For either RMCE or FLP-Beta, the toolkit is intended to leverage genome-integrated recombinase target sites.</p> | Representing an experimental second design,<b>BBa_K2605006</b> is a prototype part intended to test our novel FLP-Beta strategy. For either RMCE or FLP-Beta, the toolkit is intended to leverage genome-integrated recombinase target sites.</p> |
Revision as of 09:02, 17 October 2018
PARTS
Basic Parts
BBa_K2605000- mCherry + BGH
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BBa_K2605001- CMV with 5' SalI restriction site
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BBa_K2605002- Multiple cloning site with flanking FRT sites
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BBa_K2605003- A2UCOE
BBa_K2605004- Chicken beta-globin insulator
BBa_K2605005- FRT2
BBa_K2605006- Hybrid FlpO-beta resolvase
Composite Parts
BBa_K2605007- CMV with 5' SalI restriction site + monomeric RFP optimized for bacteria
BBa_K2605008- CMV + monomeric RFP optimized for bacteria
BBa_K2605009- CMV with 5' SalI restriction site + mCherry + BGH
BBa_K26050010- CMV + mCherry + BGH
Parts Collection
Parts BBa_K2605000 to BBa_K2605004 and BBa_K2605009 comprise the first iteration of a novel toolkit for targeted gene integration and maintenance of expression in eukaryotic chassis. The collection contains chromatin modifying elements that limit silencing of the integrated gene and minimize neighborhood effects. These elements, as well as the mCherry-BGH reporter gene with our improved CMV promoter, have restriction sites for directional cloning into part BBa_K2605002, which is a Multiple Cloning Site (MCS) flanked by distinct FRT (FLP recombinase recognition target) sites. The MCS carries sites for an arbitrary construct to be directionally cloned.
In the first iteration of our gene integration strategy, the FRT sites are leveraged for recombinase-mediated casette exchange (RMCE). Representing an experimental second design,BBa_K2605006 is a prototype part intended to test our novel FLP-Beta strategy. For either RMCE or FLP-Beta, the toolkit is intended to leverage genome-integrated recombinase target sites.