Wisconsin: Lignin Project/9 July 2008

From 2008.igem.org

(Difference between revisions)

Latest revision as of 03:24, 29 October 2008

Team Sorbitol:

The sequencing was cleaned with Agencourt CleanSEQ dye-Terminator removal).
It was then taken to the UW-biotech center for sequencing.
Start PCR the srl operon from MG1655. Run on gel and no band is formed.
Attended the Wisconsin iGEM team meeting.
Team Fungus:
Transformed PGEm-T Easy ligated with PCR2 product into DH5alpha.
Lab meeting.
Ran gradient PCR using Taq with purified PCR product from 6/24.

@@ Line 1: / Line 1: @@
-== Team Sorbitol ==
+<div style="background: #000; padding: 10px;">
-The sequencing was cleaned with Agencourt CleanSEQ dye-Terminator removal).
+<div style="width:800px; height:147px; border:0px; margin:0px;">[[Image:Igemwibanner.gif]]</div>
-It was then taken to the UW-biotech center for sequencing.
+{|align="justify" style="color:#aada84;background-color:#000;" width="800 px"
+|'''Team Sorbitol:'''<br>
-Attended the Wisconsin iGEM team meeting.
+The sequencing was cleaned with Agencourt CleanSEQ dye-Terminator removal).<br>
+It was then taken to the UW-biotech center for sequencing.<br>
+Start PCR the srl operon from MG1655. Run on gel and no band is formed. <br>
+Attended the Wisconsin iGEM team meeting.<br>
+'''Team Fungus:'''<br>
+Transformed PGEm-T Easy ligated with PCR2 product into DH5alpha.<br>
+Lab meeting.<br>
+Ran gradient PCR using Taq with purified PCR product from 6/24.<br>
+|}