Testing Results

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Line 16: Line 16:
[[Oct 8, 2006]]
[[Oct 8, 2006]]
<ul>
<ul>
-
     <li>IPTG Induction of mRFP
+
     <li>Module 1 (DH5a): IPTG Induction of mRFP
-
     <li>Arabinose Induction of LacI ts and repression of GFP
+
     <li>Module 1 (DH5a): Arabinose Induction of LacI ts and repression of GFP
</ul>
</ul>
[[Oct 7, 2006]]
[[Oct 7, 2006]]
<ul>
<ul>
-
     <li>IPTG Induction of GFP
+
     <li>Module 1 (DH5a-z1): IPTG Induction of GFP
-
     <li>Arabinose Induction of LacI ts and repression of GFP
+
     <li>Module 1 (DH5a): Arabinose Induction of LacI ts and repression of GFP
</ul>
</ul>
[[Sept 21, 2006]]
[[Sept 21, 2006]]
<ul>
<ul>
-
     <li>Module 1: IPTG Induction of GFP/mRFP
+
     <li>Module 1 (DH5a-z1): IPTG Induction of GFP/mRFP
</ul>
</ul>
[[Sept 16, 2006]]
[[Sept 16, 2006]]
<ul>
<ul>
-
     <li>Module 1: IPTG Induction of GFP
+
     <li>Module 1 (DH5a-z1): IPTG Induction of GFP
</ul>
</ul>

Revision as of 05:52, 13 October 2006

Overview

We decided to integrate check-points into our construction plan, in order to test intermediary part functionality.
There are three basic modules:

  • Module 1: Arabinose inducible pBad/araC promoter (I0500) produces temperature-sensitive LacI (LacI ts), which then, upon dimerization, represses the IPTG inducible LacI+ pL promoter (R0011) resulting in a decrease in GFP (E0240)/mRFP (I13507)
  • Module 2: In Module 1, insert DNA sequence coding for 434 cI protein instead of the reporters (GFP/mRFP) and then add Prm+ promoter (I12006), which is repressed by 434 cI and add GFP
  • Module 3: Take Module 3 and add mRFP (J04450)

Recent Tests

Oct 8, 2006

  • Module 1 (DH5a): IPTG Induction of mRFP
  • Module 1 (DH5a): Arabinose Induction of LacI ts and repression of GFP

Oct 7, 2006

  • Module 1 (DH5a-z1): IPTG Induction of GFP
  • Module 1 (DH5a): Arabinose Induction of LacI ts and repression of GFP

Sept 21, 2006

  • Module 1 (DH5a-z1): IPTG Induction of GFP/mRFP

Sept 16, 2006

  • Module 1 (DH5a-z1): IPTG Induction of GFP
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