Difference between revisions of "Team:Munich/thisisatest.html"

m
Line 2: Line 2:
 
<div class="event-info">
 
<div class="event-info">
  
<h3>Transforming E.Coli NEB Turbo to amplify plasmids for pRED/ET Engineering</h3>
+
<h3>5/18</h3>
 +
<h4>Transforming E.Coli NEB Turbo to amplify plasmids for pRED/ET Engineering</h4>
 
<table class="table table-borderless">
 
<table class="table table-borderless">
 
     <tr>
 
     <tr>
Line 23: Line 24:
 
</table>
 
</table>
  
 
+
<h3>5/24</h3>
<h3>Transforming E.Coli NEB Turbo to amplify plasmids for pRED/ET Engineering</h3>
+
<h4>Transforming E.Coli NEB Turbo to amplify plasmids for pRED/ET Engineering</h4>
 
<table class="table table-borderless">
 
<table class="table table-borderless">
 
     <tr>
 
     <tr>
Line 46: Line 47:
  
  
 
+
<h3>5/25</h3>
<h3>Transforming E.Coli NEB Turbo to amplify plasmids for pRED/ET Engineering</h3>
+
<h4>Transforming E.Coli NEB Turbo to amplify plasmids for pRED/ET Engineering</h4>
 
<table class="table table-borderless">
 
<table class="table table-borderless">
 
     <tr>
 
     <tr>
Line 68: Line 69:
 
</table>
 
</table>
  
 
+
<h3>5/26</h3>
<h3>DNA preparation for pRED/ET Engineering</h3>
+
<h4>DNA preparation for pRED/ET Engineering</h4>
 
<table class="table table-borderless">
 
<table class="table table-borderless">
 
     <tr>
 
     <tr>

Revision as of 15:34, 14 September 2018

5/18

Transforming E.Coli NEB Turbo to amplify plasmids for pRED/ET Engineering

Participants: Dominic
Protocol: epo. Trafo
Notes: inoculate pRED at 30°C because of temperature sensitive promoter
Results: no colonies

5/24

Transforming E.Coli NEB Turbo to amplify plasmids for pRED/ET Engineering

Participants: Dominic
Protocol: epo. Trafo
Notes: inoculate pRED at 30°C because of temperature sensitive promoter, pKD3 contains resistance cassette flanked by FRT sites
Results: no colonies


5/25

Transforming E.Coli NEB Turbo to amplify plasmids for pRED/ET Engineering

Participants: Dominic
Protocol: chem. Trafo
Notes: pKD3 contains resistance cassette flanked by FRT sites
Results: no colonies

5/26

DNA preparation for pRED/ET Engineering

Participants: Dominic
Protocol: mini prep
Notes: because pRED/ET could not be transformed, we got readily transformed cells from PD Dr. Jürgen Lassak from the LMU
Results: pRED/ET: 37,5 ng/ul

pNPTS138-R6KT: 60ng/ul