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| <li><a name="scaffold0" >Overview</a></li> | | <li><a name="scaffold0" >Overview</a></li> |
| <li><a name="scaffold1" >RNA Scaffold Design</a></li> | | <li><a name="scaffold1" >RNA Scaffold Design</a></li> |
- | <li><a name="scaffold2" >RNA Scaffold Data</a></li>
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| <li><a name="scaffold3" >PUF Tethering Design</a></li> | | <li><a name="scaffold3" >PUF Tethering Design</a></li> |
- | <li><a name="scaffold4" >PUF Tethering Data</a></li>
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| <li><a name="scaffold5" >Conclusion</a></li> | | <li><a name="scaffold5" >Conclusion</a></li> |
| </div> | | </div> |
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| <div id="scaffold1" style="display:none"> | | <div id="scaffold1" style="display:none"> |
| <center><h2>RNA Scaffold Design</h2></center> | | <center><h2>RNA Scaffold Design</h2></center> |
- | </div>
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- | <div id="scaffold2" style="display:none">
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- | <center><h2>RNA Scaffold Data</h2></center>
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- | <center>
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- | <img src="https://static.igem.org/mediawiki/2012/9/95/Lysate_gel.png" height=100% width=100%></center>
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- | <br/><b>Fig. 1.</b> 1 L culture incubated at 37oC till 0.5 nm optical density after inoculation with 5 mL of overnight for WT PUF-PIN and 6-2/7-2 PUF-PIN. 2 mM IPTG induction for 2 hours. 200 mL cultures incubated at 37oC till 1 nm optical density after inoculation with 2 mL of overnight for WT PUF-αGFP cultures. 2 mM IPTG induction for various hours.
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- | <br/><br/>
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- | <center>
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- | <img src="https://static.igem.org/mediawiki/2012/4/41/WT_PUF-PIN_Protein_Purification.png" height=100% width=100%></center>
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- | <br/><b>Fig. 2.</b> 1 L culture incubated at 37oC till 0.5 nm optical density after inoculation with 5 mL of overnight. 2 mM IPTG induction for 2 hours. His-Tag Ni-NTA purification, centrifuged with Millipore 30kDa cutoff ultracentrifuge tubes.
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- | <br/><br/>
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- | <center>
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- | <img src="https://static.igem.org/mediawiki/2012/6/6f/6-2%2C7-2_PUF-PIN_Protein_Purification.png" height=100% width=100%></center>
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- | <br/><b>Fig. 3.</b> 1 L culture incubated at 37oC till 0.5 nm optical density after inoculation with 5 mL of overnight. 2 mM IPTG induction for 2 hours. His-Tag Ni-NTA purification, centrifuged with Millipore 30kDa cutoff ultracentrifuge tubes.
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- | <br/><br/>
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- | <center><img src="https://static.igem.org/mediawiki/2012/f/ff/IVT_gel.jpg" height=100% width=100%><br/>
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- | </center>
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- | <b>Fig. 4.</b> In-Vitro Transcription with MEGAscript® T7 Kit (Invitrogen)
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- | <br/><br/>
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| </div> | | </div> |
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| <div id="scaffold3" style="display:none"> | | <div id="scaffold3" style="display:none"> |
| <center><h2>PUF Tether Design</h2></center> | | <center><h2>PUF Tether Design</h2></center> |
- | </div>
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- | <div id="scaffold4" style="display:none">
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- | <center><h2>PUF Tethering Data</h2></center>
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- | <center>
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- | <br/>
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- | <img src="https://static.igem.org/mediawiki/2012/d/d4/Tether1.jpg" height=50% width=50%>
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- | <br/><b>Fig 1.</b>
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- | <br/><br/>
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- | <img src="https://static.igem.org/mediawiki/2012/b/b1/Tether2.jpg" height=50% width=50%>
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- | <br/><b>Fig 2.</b>
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- | <br/><br/>
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- | <img src="https://static.igem.org/mediawiki/2012/c/cf/Tether3.jpg" height=50% width=50%>
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- | <br/><b>Fig 3.</b>
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- | <br/><br/>
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- | <img src="https://static.igem.org/mediawiki/2012/b/b6/Tether4.jpg" height=50% width=50%>
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- | <br/><b>Fig 4.</b>
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- | <br/><br/>
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- | <img src="https://static.igem.org/mediawiki/2012/f/f5/Tether5.jpg" height=50% width=50%>
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- | <br/><b>Fig 5.</b>
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- | <br/><br/></center>
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| </div> | | </div> |
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