Team:St Andrews/Procedure
From 2012.igem.org
(Difference between revisions)
Line 535: | Line 535: | ||
<p>For primer annealing in the PCR, the primer sequences were combined in the following way:</p> | <p>For primer annealing in the PCR, the primer sequences were combined in the following way:</p> | ||
- | <li>GST Forward and Ni Reverse</li> | + | <li><strong>GST Forward</strong> and <strong>Ni Reverse</strong></li> |
- | <li>GST Forward | + | <li><strong>GST Forward</strong> and <strong>Ni<sub>2</sub> Reverse</strong></li> |
- | <li>GST Forward | + | <li><strong>GST Forward</strong> and <strong>Pd Reverse</strong></li> |
- | <li>GST Forward | + | <li><strong>GST Forward</strong> and <strong>Pt Reverse</strong></li> |
- | + | ||
<BR> </BR> | <BR> </BR> |
Revision as of 14:42, 27 July 2012
Lab Book
Procedure
- date
- what we did
- date
- what we did
- date
- what we did
anyone really keen to write this up, up to protein visualization? Don't forget to mention the differing restriction enzymes and vectors of each team. I can add in links to the protocols page.
Please also refer to our Protocols page.
Sequences Primers Sequencing results Lipid analysis
Start from lipid extraction
primers, sequence results
Sequences