Team:Warsaw/Calendar-Main/3 July 2008

From 2008.igem.org

(Difference between revisions)
 
(4 intermediate revisions not shown)
Line 3: Line 3:
<html>
<html>
-
<h3>Change of the reporter from pZC with B-galactosidaze to GFP or RFP</h3>
+
<h3>Change of the reporter from <a href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pZC320>pZC320</a> with B-galactosidase to GFP or RFP</h3>
<h4>Piotr, Weronika</h4>
<h4>Piotr, Weronika</h4>
<ol>
<ol>
-
<li>There were blue and white colonies but no red or green in UV</li>
+
<li>There were blue and white colonies but no red or green fluorescence in UV.</li>
-
<li>Inoculation of liquid LB medium + Amp with white colonies</li>
+
<li>Inoculation of liquid LB medium + Amp with white colonies.</li>
</li></ol>
</li></ol>
-
<h3>Preparation of constructs with OmpA protein fusions</h3>
+
<h3>Preparation of constructs on pET15b: OmpA_alpha and OmpA_omega</h3>
<h4>Paweł</h4>
<h4>Paweł</h4>
<p>
<p>
-
Colonies of each transformants from previous day (<a href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pET15b%2BOmpA-alpha>pET15b+OmpA_alpha</a> and <a href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pET15b%2BOmpA-omega>pET15b+OmpA_omega</a>) were inoculated to liquid LB + ampicillin.</p>
+
Colonies from each transformant strain from previous day (<a href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pET15b%2BOmpA-alpha>pET15b+OmpA_alpha</a> and <a href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pET15b%2BOmpA-omega>pET15b+OmpA_omega</a>) were inoculated to liquid LB + ampicillin.</p>
<h3>Cloning alpha-A and omega-A fusions on <a href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pKSII%2B>pKS</a></h3>
<h3>Cloning alpha-A and omega-A fusions on <a href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pKSII%2B>pKS</a></h3>
<h4>Michał L., Ewa, Marcin</h4>
<h4>Michał L., Ewa, Marcin</h4>
-
<p>We have received sequencing results: A is OK but in case of Alpha-A and Omega-A the result is weird. It seems that there were error in synthesis of OmegaP+link10+homo2 and AlphaP+link10+homo2 primer which causes frameshift and cloning of these fusions have to be repeated from the beginning.</p>
+
<p>We have received sequencing results: A is OK but in case of Alpha-A and Omega-A the result is weird. It seems that there were error in synthesis of OmegaP+link10+homo2 and AlphaP+link10+homo2 primers which causes frameshift and cloning of these fusions has to be repeated from the beginning.</p>
</html>
</html>

Latest revision as of 14:07, 28 October 2008

Gallery Bricks Notebook Team Project Home


Previous day
return to main notebook page
Previous entry
next notebook entry

 


Change of the reporter from pZC320 with B-galactosidase to GFP or RFP

Piotr, Weronika

  1. There were blue and white colonies but no red or green fluorescence in UV.
  2. Inoculation of liquid LB medium + Amp with white colonies.

Preparation of constructs on pET15b: OmpA_alpha and OmpA_omega

Paweł

Colonies from each transformant strain from previous day (pET15b+OmpA_alpha and pET15b+OmpA_omega) were inoculated to liquid LB + ampicillin.

Cloning alpha-A and omega-A fusions on pKS

Michał L., Ewa, Marcin

We have received sequencing results: A is OK but in case of Alpha-A and Omega-A the result is weird. It seems that there were error in synthesis of OmegaP+link10+homo2 and AlphaP+link10+homo2 primers which causes frameshift and cloning of these fusions has to be repeated from the beginning.