Team:Bielefeld-Germany/Labjournal/August

From 2013.igem.org

(Difference between revisions)
Line 29: Line 29:
<h4><a href="https://2013.igem.org/Team:Bielefeld-Germany/Project/Cytochromes">Cytochromes</a></h4>
<h4><a href="https://2013.igem.org/Team:Bielefeld-Germany/Project/Cytochromes">Cytochromes</a></h4>
-
<p></p>
+
<div class="cyt_restr1_hl"><p><a>Restriction of ccmAH and psB1C3 and Suffix-Insertion</a></p></div>
 +
<div class="cyt_retr1">
 +
<blockquote>
 +
The backbone and shipping vector psB1C3 was cut with EcoRI, SpeI, the insert ccmAH with EcoRI and XbaI  to perfom a standard suffix insertion.
 +
<br>We used approx. 200ng insert and 42ng vector, which repressnts a 2-fold molar excess of insert.
 +
<br>The Ligation was incubated for 15 min at 37°C, followed by a heat-inactivation at 80°C for 20 min.
 +
<br>The subsequent gel electrophoresis did not yield any positiv results, probably due to the use of buffer and enzymes from two different manufactures.
 +
<br>
 +
</blockquote>
 +
</div>
 +
 
 +
 
<h4><a href="https://2013.igem.org/Team:Bielefeld-Germany/BioSafety">Biosafety</a></h4>
<h4><a href="https://2013.igem.org/Team:Bielefeld-Germany/BioSafety">Biosafety</a></h4>

Revision as of 10:54, 3 September 2013






August

Milestones


1.Week

MFC

Mediators

Cytochromes

The backbone and shipping vector psB1C3 was cut with EcoRI, SpeI, the insert ccmAH with EcoRI and XbaI to perfom a standard suffix insertion.
We used approx. 200ng insert and 42ng vector, which repressnts a 2-fold molar excess of insert.
The Ligation was incubated for 15 min at 37°C, followed by a heat-inactivation at 80°C for 20 min.
The subsequent gel electrophoresis did not yield any positiv results, probably due to the use of buffer and enzymes from two different manufactures.

Biosafety

Porines









2.Week

MFC

Mediators

Cytochromes

Biosafety

Porines









3.Week

MFC

Mediators

Cytochromes

Biosafety

Porines









4.Week

MFC

Mediators

Cytochromes

Biosafety

Porines