IGEM:University of East Anglia (UEA), Norwich, UK/2009/Notebook/NRP-UEA-Norwich iGEM/2014/08/08: Difference between revisions

From OpenWetWare
Jump to navigationJump to search
Line 8: Line 8:
* Spread the level 2 constructs A-G on spectinomycin plates with IPTG and XGAL for blue white selection as well as plating the transformation of vector pAGM8031.   
* Spread the level 2 constructs A-G on spectinomycin plates with IPTG and XGAL for blue white selection as well as plating the transformation of vector pAGM8031.   


* Plated end linkers 2 and 3 on ampicillin and all plates incubated overnight at 37<sup>O</sup>C.
* Plated end linkers 2 and 3 on ampicillin and all plates incubated overnight at 37<sup>o</sup>C.


* Picked colonies of ''Agrobacterium tumerfaciens'', 2, 3, 4, 10 and 11 and grew in an overnight culture with shaking (28<sup>O</sup>C) with 400 μL LB and 1μL/mL of ampicillin.
* Picked colonies of ''Agrobacterium tumerfaciens'', 2, 3, 4, 10 and 11 and grew in an overnight culture with shaking (28<sup>o</sup>C) with 400 μL LB and 1μL/mL of ampicillin.


We invited the Cambridge iGEM team up to meet us and discuss each others projects as well as future collaborations and gave them a tour of the NRP, JIC and UEA.  We discussed providing Cambridge with our MoFlipper so they can submit their parts in BioBrick form as well.  
We invited the Cambridge iGEM team up to meet us and discuss each others projects as well as future collaborations and gave them a tour of the NRP, JIC and UEA.  We discussed providing Cambridge with our MoFlipper so they can submit their parts in BioBrick form as well.  

Revision as of 04:34, 11 August 2014

iGEM Project name 1 <html><img src="/images/9/94/Report.png" border="0" /></html> Main project page
<html><img src="/images/c/c3/Resultset_previous.png" border="0" /></html>Previous entry<html>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</html>Next entry<html><img src="/images/5/5c/Resultset_next.png" border="0" /></html>

Week 8 Day 4

  • Spread the level 2 constructs A-G on spectinomycin plates with IPTG and XGAL for blue white selection as well as plating the transformation of vector pAGM8031.
  • Plated end linkers 2 and 3 on ampicillin and all plates incubated overnight at 37oC.
  • Picked colonies of Agrobacterium tumerfaciens, 2, 3, 4, 10 and 11 and grew in an overnight culture with shaking (28oC) with 400 μL LB and 1μL/mL of ampicillin.

We invited the Cambridge iGEM team up to meet us and discuss each others projects as well as future collaborations and gave them a tour of the NRP, JIC and UEA. We discussed providing Cambridge with our MoFlipper so they can submit their parts in BioBrick form as well.

Jack met with Graeme Byrne to prepare for meeting with InCrops on the 28th of August.