Team:British Columbia/Notebook/4 July 2011

From 2011.igem.org

(Difference between revisions)
(July 04 2011)
(July 04 2011)
 
(2 intermediate revisions not shown)
Line 1: Line 1:
 +
{{Template:Notebook}}
==July 04 2011==
==July 04 2011==
-
 
+
<b>IDI1, HMG2, erg20-2</b>
-
===Week of Jun27 - Jul04===
+
-
====IDI1, HMG2, erg20-2====
+
*Validated competent cells by transforming with pet100 vector containing Cineole synthase.  They are in working order.
*Validated competent cells by transforming with pet100 vector containing Cineole synthase.  They are in working order.
*Amplified 5 plasmids received from Greece (IDI1, HMG2, p300, Cin, Sab).  NOTE: did not properly centrifuge during DNA precipitation stage.  Will validate plasmids in yeast transformations to make sure plasmids are in working order.
*Amplified 5 plasmids received from Greece (IDI1, HMG2, p300, Cin, Sab).  NOTE: did not properly centrifuge during DNA precipitation stage.  Will validate plasmids in yeast transformations to make sure plasmids are in working order.
*Awaiting materials from France (erg20-2).
*Awaiting materials from France (erg20-2).
-
 
+
<p><b>1,8-Cineole</b></p>
-
====1,8-Cineole====
+
*Ran a gel to test restriction digest on variant SDM-PCR product. Looks like the SDM was successful!
-
*Ran a gel to test restriction digest and variant SDM-PCR product.
+
<p><b>beta-pinene & (-)-limonene</b></p>
-
 
+
-
====beta-pinene====
+
*SDM beta-pinene again by using both Pfu and Taq.  
*SDM beta-pinene again by using both Pfu and Taq.  
*Gel verification shows a smear.  
*Gel verification shows a smear.  
*Troubleshooting: run a gel on the miniprep of the beta-pinene plasmid received from Rafael to make sure that the DNA hasn't been contaminated/digested.
*Troubleshooting: run a gel on the miniprep of the beta-pinene plasmid received from Rafael to make sure that the DNA hasn't been contaminated/digested.

Latest revision as of 20:04, 30 July 2011

Team: British Columbia - 2011.igem.org

July 04 2011

IDI1, HMG2, erg20-2

  • Validated competent cells by transforming with pet100 vector containing Cineole synthase. They are in working order.
  • Amplified 5 plasmids received from Greece (IDI1, HMG2, p300, Cin, Sab). NOTE: did not properly centrifuge during DNA precipitation stage. Will validate plasmids in yeast transformations to make sure plasmids are in working order.
  • Awaiting materials from France (erg20-2).

1,8-Cineole

  • Ran a gel to test restriction digest on variant SDM-PCR product. Looks like the SDM was successful!

beta-pinene & (-)-limonene

  • SDM beta-pinene again by using both Pfu and Taq.
  • Gel verification shows a smear.
  • Troubleshooting: run a gel on the miniprep of the beta-pinene plasmid received from Rafael to make sure that the DNA hasn't been contaminated/digested.