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Team:ZJU-China/Processing
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| + | <b><big><big><big><big><center>Working process of GeneSocket</center></big></big></big></big></b><br /> | ||
| + | <p style="font-size:13pt">Look through this page, and you will understand the working process of GeneSocket inside the cell and learn corresponding experiment step.</p> | ||
| - | <table class="img" style="float:none;width:100%;font-size:14pt;"> | + | |
| - | <tr><th width="50%">Details in Socket E.coli</th><th width="50%">Tasks for you</th></tr> | + | <table border=1px class="img" cellspacing="0" bordercolorlight="#333333" bordercolordark="#efefef" style="float:none;width:100%;font-size:14pt;" > |
| - | <tr><td></td><td><p>Design circuit and find your parts DNA</p></td></tr> | + | <tr bgcolor=#cccccc><th width="50%">Details in Socket E.coli</th><th width="50%">Tasks for you</th></tr> |
| - | <tr><td></td><td><p>Use GS-BOX to design the strategy of circuit construction</p></td></tr> | + | <tr bgcolor=#eafeff><td></td><td><p>Design circuit and find your parts DNA</p></td></tr> |
| - | <tr><td></td><td><p>PCR to add Homeoregion, Ligase standard parts.</p></td></tr> | + | <tr bgcolor=#eafeff><td></td><td><p>Use GS-BOX to design the strategy of circuit construction</p></td></tr> |
| - | <tr><td><p>Lambda red protein is expressed during cultivation</p></td><td><p>Making electrotranformation competent cells, use reporter 1 to select.</p></td></tr> | + | <tr bgcolor=#eafeff><td></td><td><p>PCR to add Homeoregion, Ligase standard parts.</p></td></tr> |
| - | <tr><td><p>Inserted circuit(dsDNA) are introduced into Socket.coli.</p></td><td><p>electrotranformation</p></td></tr> | + | <tr bgcolor=#eafeff><td><p>Lambda red protein is expressed during cultivation</p></td><td><p>Making electrotranformation competent cells, use reporter 1 to select.</p></td></tr> |
| - | <tr><td><p>Inserted circuit recombine biterminator unit<br> | + | <tr bgcolor=#eafeff><td><p>Inserted circuit(dsDNA) are introduced into Socket.coli.</p></td><td><p>electrotranformation</p></td></tr> |
| - | <img src="https://static.igem.org/mediawiki/2014/ | + | <tr bgcolor=#eafeff><td><p>Inserted circuit recombine biterminator unit<br> |
| - | <tr><td><p>Int express after recombination, flip over attB/attP site</p></td></tr> | + | <img src="https://static.igem.org/mediawiki/2014/4/4c/Zju-rep-Int-exp.gif" width="270" height="200" align ="center" style="float:none"/></p></td><td rowspan="2"><p>Cell recovery after electrotranformation, liquid cultivation.</p></td></tr> |
| - | <tr><td><p>Stage switched, reporter 2 expressed | + | <tr bgcolor=#eafeff><td><p>Int express after recombination, flip over attB/attP site</p></td></tr> |
| - | <img src="https://static.igem.org/mediawiki/2014/ | + | <tr bgcolor=#eafeff><td><p>Stage switched, reporter 2 expressed |
| + | <img src="https://static.igem.org/mediawiki/2014/b/bc/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 bgcolor=#eafeff><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/ | + | <img src="https://static.igem.org/mediawiki/2014/6/6b/Zju-int-xis-flip-lr.gif " width="270" height="200" align ="center" style="float:none"/> |
| - | + | <p> </p><p> </p> | |
| + | <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 bgcolor=#eafeff><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>If circuit construction is over, cultivate cell in 42℃ to discard Support device.</p></td></tr> | + | <tr bgcolor=#eafeff><td></td><td><p>If circuit construction is over, cultivate cell in 42℃ to discard Support device.</p></td></tr> |
</table> | </table> | ||
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| + | <!--embed width="320" height="240" controls="controls" src="https://static.igem.org/mediawiki/2014/4/4e/ZJU_Full_cartoon.mov" autostart="false" loop="false"></embed--> | ||
| + | <!--video width="320" height="240" controls="controls"> | ||
| + | <source src="https://static.igem.org/mediawiki/2014/4/4e/ZJU_Full_cartoon.mov" type="video/mov" /></video--></p> | ||
| + | <img src="https://static.igem.org/mediawiki/2014/1/1e/ZJU_Full.gif" width="100%" style="float:none"> | ||
| + | <table> | ||
| + | <tr> | ||
| + | <td><img src="https://static.igem.org/mediawiki/2014/4/47/ZJU_left_arow.png"> </img></td><td> <a href="https://2014.igem.org/Team:ZJU-China/GeneSocket">Previous: GeneSocket</a></td> | ||
| + | <td width=600px></td> | ||
| + | <td><a href="https://2014.igem.org/Team:ZJU-China/Design">Next: Circuit Design</a> </td><td><img src="https://static.igem.org/mediawiki/2014/1/19/ZJU_right_arow.png" > </img> </td> | ||
| + | </tr> | ||
| + | </table> | ||
</div> | </div> | ||
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</html> | </html> | ||
Latest revision as of 03:36, 18 October 2014
| Team Sponsor | Contact us | ||
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Team Forum(BBS): | ZJU-China 2014 Team Forum on www.zjubiolab.zju.edu.cn | |
| Post Address: | Biolab Center Room 413, ZJU Zijin'gang Campus, Yuhang Tang Road No.866, Hangzhou, Zhejiang |
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| Powered by Media Wiki. Zhejiang University. | Email Address: | zjuchina2014 @ 163.com | |
Look through this page, and you will understand the working process of GeneSocket inside the cell and learn corresponding experiment step.
| 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. |
 | Previous: GeneSocket | Next: Circuit Design |  |
