Team:ZJU-China/Processing
From 2014.igem.org
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<tr><td><p>Int express after recombination, flip over attB/attP site</p></td></tr> | <tr><td><p>Int express after recombination, flip over attB/attP site</p></td></tr> | ||
<tr><td><p>Stage switched, reporter 2 expressed | <tr><td><p>Stage switched, reporter 2 expressed | ||
- | <img src="https://static.igem.org/mediawiki/2014/7/74/ZJU_int_flip_bp.gif" width="270" height="200" align ="center"/> | + | <img src="https://static.igem.org/mediawiki/2014/7/74/ZJU_int_flip_bp.gif" width="270" height="200" align ="center" style="float:none"/> |
</p></td><td><p>plate cultivation, Use reporter 2 to select candidate cells</p></td></tr> | </p></td><td><p>plate cultivation, Use reporter 2 to select candidate cells</p></td></tr> | ||
<tr><td><p>Xis express, Int+Xis will flip over attL/attR sites. Stage switched again and inverted biterminator unit flipped over to silence Int expression | <tr><td><p>Xis express, Int+Xis will flip over attL/attR sites. Stage switched again and inverted biterminator unit flipped over to silence Int expression | ||
- | <img src="https://static.igem.org/mediawiki/2014/4/4c/Zju_int_xis_flip_lr.gif " width="270" height="200" align ="center"/> | + | <img src="https://static.igem.org/mediawiki/2014/4/4c/Zju_int_xis_flip_lr.gif " width="270" height="200" align ="center" style="float:none"/> |
<p> </p><p> </p> | <p> </p><p> </p> | ||
- | <img src="https://static.igem.org/mediawiki/2014/2/2b/ZJU_Teminator_flipover.gif" width="270" height="200" align ="center"/> | + | <img src="https://static.igem.org/mediawiki/2014/2/2b/ZJU_Teminator_flipover.gif" width="270" height="200" align ="center" style="float:none"/> |
</p></td><td><p><b>select positive colony to amplify, Arabinose induce at the main time. Use plasmid backbone resistance to select.</b></p></td></tr> | </p></td><td><p><b>select positive colony to amplify, Arabinose induce at the main time. Use plasmid backbone resistance to select.</b></p></td></tr> | ||
<tr><td></td><td><p>plate cultivation, Use reporter 1 to select candidate cells. This survival cells are ready for the next recombination round.</p></td></tr> | <tr><td></td><td><p>plate cultivation, Use reporter 1 to select candidate cells. This survival cells are ready for the next recombination round.</p></td></tr> | ||
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<p> | <p> | ||
<video width="320" height="240" controls="controls"> | <video width="320" height="240" controls="controls"> | ||
- | <source src="https://static.igem.org/mediawiki/2014/4/4e/ZJU_Full_cartoon.mov" type="video/ | + | <source src="https://static.igem.org/mediawiki/2014/4/4e/ZJU_Full_cartoon.mov" type="video/mov" /></video></p> |
</div> | </div> |
Revision as of 00:03, 18 October 2014
Details in Socket E.coli | Tasks for you |
---|---|
Design circuit and find your parts DNA | |
Use GS-BOX to design the strategy of circuit construction | |
PCR to add Homeoregion, Ligase standard parts. | |
Lambda red protein is expressed during cultivation | Making electrotranformation competent cells, use reporter 1 to select. |
Inserted circuit(dsDNA) are introduced into Socket.coli. | electrotranformation |
Inserted circuit recombine biterminator unit | Cell recovery after electrotranformation, liquid cultivation. |
Int express after recombination, flip over attB/attP site | |
Stage switched, reporter 2 expressed | plate cultivation, Use reporter 2 to select candidate cells |
Xis express, Int+Xis will flip over attL/attR sites. Stage switched again and inverted biterminator unit flipped over to silence Int expression
| select positive colony to amplify, Arabinose induce at the main time. Use plasmid backbone resistance to select. |
plate cultivation, Use reporter 1 to select candidate cells. This survival cells are ready for the next recombination round. | |
If circuit construction is over, cultivate cell in 42℃ to discard Support device. |