Team:Heidelberg/Notebook/Sensing Group/Notebook/9thweek

From 2008.igem.org

(Difference between revisions)
(Wednesday, 10/01/2008)
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* Miniprep of Fusion-LuxP-pBAD33 (both constructs)
* Miniprep of Fusion-LuxP-pBAD33 (both constructs)
* Digestion of pSB1A3 with EcoRI,PstI,NdeI (3µl DNA, 40 µl total volume)
* Digestion of pSB1A3 with EcoRI,PstI,NdeI (3µl DNA, 40 µl total volume)
-
* Digestion of pSB2K3 (10µl DNA, 20µl total volume) with EcoRI,PstI  
+
* Digestion of pSB2K3 (10µl DNA, 20µl total volume) with EcoRI,PstI
 +
[[Image:HD 081001-F-PCR prefix speI.png|center|thumb|400px|PCR GeneArt Fusion constructs with Prefix/Suffix primer yielded no product. F1/F2 with prefix/speI primer were positive, but mutation strategy dropped later. A mix of LuxS and pDK6 was added on the gel to check if double transformation was successfull. Digestions of pSB1A3 and pSB2K3 with EcoRI/Pst were supposed to be used for subsequent standardization of parts]]
== Thursday, 10/02/2008 ==
== Thursday, 10/02/2008 ==

Revision as of 19:28, 26 October 2008

Back to the overview


Contents

Tuesday, 09/30/2008

  • Miniprep of LuxS+pDK6 and F1/F2-Luxp-pBAD33
  • Digestion of GeneArt Fusion constructs with EcoRI/PstI and Gel-Extraction
  • Digestion of GeneArt Fusion constructs with EcoRI/PstI and Gel-Extraction

Wednesday, 10/01/2008

  • Miniprep of Fusion-LuxP-pBAD33 (both constructs)
  • Digestion of pSB1A3 with EcoRI,PstI,NdeI (3µl DNA, 40 µl total volume)
  • Digestion of pSB2K3 (10µl DNA, 20µl total volume) with EcoRI,PstI
PCR GeneArt Fusion constructs with Prefix/Suffix primer yielded no product. F1/F2 with prefix/speI primer were positive, but mutation strategy dropped later. A mix of LuxS and pDK6 was added on the gel to check if double transformation was successfull. Digestions of pSB1A3 and pSB2K3 with EcoRI/Pst were supposed to be used for subsequent standardization of parts

Thursday, 10/02/2008

Friday, 10/03/2008

Go to 10th week