Team:Warsaw/Calendar-Main/11 July 2008

From 2008.igem.org

(Difference between revisions)
 
(29 intermediate revisions not shown)
Line 1: Line 1:
{{WarNotebook}}
{{WarNotebook}}
<!-- do not edit above me! -->
<!-- do not edit above me! -->
 +
<html>
-
<p>'''Preparation of constructs with OmpA protein fusions'''<br>
+
<h3>Preparation of construct <a href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pKSII+A>pKS with A protein</a></h3>
-
1. Colony PCR on colonies from plates with transformations OmpA_alpha. <br>
+
<h4>Michał L., Ewa, Marcin</h4>
-
2. Confirmed transformant colonies inoculated to liquid LB with kanamycin.<br>
+
<p><ol>
-
'''Cloning of protein Z DNA to OmpA constructs''' <br>
+
<li> Colony PCR on colonies from plates with transformations <a href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pKSII+A>pKS-A</a>. <br>
-
1. 2 colonies was inoculated to liquid LB broth with kanamycin<br>
+
Primers used:
-
'''Preparation of construct omega-A'''<br>
+
-
<br>
+
-
1. PCR A in 50 µl<br>
+
-
template DNA - pKS-A4 1 µl<br>
+
-
primer <html>
+
-
<a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#AP+NotI_N">AP+NotI_N</a></html> - 2 µl<br>
+
-
primer<html>
+
-
<a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#AL+link10+homo2_N">AL+link10+homo2_N</a></html> - 2 µl<br>
+
-
Pfu polymerase buffer + Mg2+ (from Fermentas) - 5 µl<br>
+
-
dNTPs - 1 µl <br>
+
-
Pfu turbo - 0.5 µl<br>
+
-
H2o - 38.5 µl<br>
+
-
<br>
+
-
program:<br>
+
-
1. 95&deg;C 3'<br>
+
-
2. 95&deg;C 30"<br>
+
-
3.62&deg;C 45"<br>
+
-
4.72&deg;C 45"<br>
+
-
5.72&deg;C 10'<br>
+
-
6. keeping in 4&deg;C<br>
+
-
<br>
+
-
2. PCR omega in 50 µl<br>
+
-
template DNA - pUC19 1 µl<br>
+
-
primer OmegaLS - 2 µl<br>
+
-
primer AOmegaPli - 2 µl<br>
+
-
Pfu polymerase buffer + Mg2+ (from Fermentas) - 5 µl<br>
+
-
dNTPs - 1 µl <br>
+
-
Pfu turbo - 0.5 µl<br>
+
-
H2o - 38.5 µl<br>
+
-
<br>
+
-
program:
+
-
1. 95&deg;C 3'<br>
+
-
2. 95&deg;C 30"<br>
+
-
3. 62&deg;C 45"<br>
+
-
4. 72&deg;C 45"<br>
+
-
5. 72&deg;C 10'<br>
+
-
6. keeping in 4&deg;C<br>
+
-
25 cycles
+
-
<br>
+
-
3. gel electrophoresis<br>
+
-
<br>
+
-
4.reisolation from agarose gel<br>
+
-
</p>
+
 +
<a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#AL+SacI">AL+SacI</a> and <a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#AP+NotI">AP+NotI</a>
 +
</li><li> Gel electrophoresis.</li>
 +
<li> Confirmed transformant colonies inoculated to liquid LB with ampicillin.</li></ol></p>
 +
 +
 +
 +
<h3>Cloning of protein Z DNA to <a href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pET15b%2BOmpA-alpha>pET15b-OmpA-alpha</a> in place of OmpA</h3>
 +
<h4>Piotr, Antoni</h4>
 +
<p><a href=https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#plasmid_DNA_isolation>Isolation</a> of plasmids from cultures inoculated on previous day.</p>
 +
 +
<h3>Preparation of constructs: OmpA_alpha and OmpA_omega #2</h3>
 +
 +
<h4>Michał K.</h4>
 +
<p><ol>
 +
<li> Colony <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#pcr">PCR</a> with <a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#OmpaL_N">OmpaL_N</a> and <a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#OmpaP_link">OmpaP_link</a>
 +
 +
primers on colonies from plates with transformations OmpA_alpha (annealing temperature - 55&deg;C,45 s of elongation step). </li>
 +
<li> Gel electrophoresis (<a href="https://2008.igem.org/Team:Warsaw/Calendar-Main/11_July_2008#fig1">Fig. 1.</a>).</li>
 +
<li> Confirmed transformant colonies inoculated to liquid LB with kanamycin.</li>
 +
</ol></p>
 +
 +
 +
<a name="fig1"><img src="https://static.igem.org/mediawiki/2008/7/7e/11_th_july.jpg" width=300 /></a><var><b>Fig. 1. </b>Colony PCR using: OmpaL_N and OmpaP_link primers<b></b><br>
 +
Upper<br>
 +
1. Marker<br>
 +
2-13. colony PCR products carrying probable OmpA-alpha<br>
 +
Lower<br>
 +
1. Marker<br>
 +
2-13. colony PCR products carrying probable OmpA-alpha<br></var>
 +
 +
 +
</html>
<!-- do not remove this! -->
<!-- do not remove this! -->
{{WarNotebookEnd}}
{{WarNotebookEnd}}

Latest revision as of 17:44, 26 October 2008

Gallery Bricks Notebook Team Project Home


Previous day
return to main notebook page
Previous entry
Interactive list of topics
next notebook entry

 


Preparation of construct pKS with A protein

Michał L., Ewa, Marcin

  1. Colony PCR on colonies from plates with transformations pKS-A.
    Primers used: AL+SacI and AP+NotI
  2. Gel electrophoresis.
  3. Confirmed transformant colonies inoculated to liquid LB with ampicillin.

Cloning of protein Z DNA to pET15b-OmpA-alpha in place of OmpA

Piotr, Antoni

Isolation of plasmids from cultures inoculated on previous day.

Preparation of constructs: OmpA_alpha and OmpA_omega #2

Michał K.

  1. Colony PCR with OmpaL_N and OmpaP_link primers on colonies from plates with transformations OmpA_alpha (annealing temperature - 55°C,45 s of elongation step).
  2. Gel electrophoresis (Fig. 1.).
  3. Confirmed transformant colonies inoculated to liquid LB with kanamycin.

Fig. 1. Colony PCR using: OmpaL_N and OmpaP_link primers
Upper
1. Marker
2-13. colony PCR products carrying probable OmpA-alpha
Lower
1. Marker
2-13. colony PCR products carrying probable OmpA-alpha

Retrieved from "http://2008.igem.org/Team:Warsaw/Calendar-Main/11_July_2008"