Team:Warsaw/Calendar-Main/24 July 2008

From 2008.igem.org

(Difference between revisions)
Line 38: Line 38:
<li>We have obtained white colonies of transformants and inoculated 10 of them on liquid LB+Amp<sub>100</sub></li>
<li>We have obtained white colonies of transformants and inoculated 10 of them on liquid LB+Amp<sub>100</sub></li>
-
<h3>Cloning of protein Z DNA to pET15b-OmpA-omega in place of OmpA<br>
 
-
Paweł</h3>
 
-
<p><ol><li>Result of transformation of pET15b+omega with protein Z DNA: 4 colonies grown</li>
 
-
<li>Each colony cultured overnight in LB+amp</li>
 
-
</ol>
 
-
</p>
 
-
<h3> Michał L., Ewa, Marcin</h3>
+
 
-
We have finally got rid of phage infection and we are able to work with E. coli again. Hurray!
+
 
</html>
</html>

Revision as of 18:33, 11 October 2008

Gallery Bricks Notebook Team Project Home


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

 



  1. Separate transformant colonies (tranformation of ligation of pACYC177+OmpA_alpha and omega_A from previous day) inoculated to liquid LB with kanamycin.

Antoni:

  1. Preparation of chemocompetent bacteria E. coli TOP10.

Cloning omega-A fusion on pKS (second attempt)

Michał L., Ewa, Marcin:

Sequencing confirms that we have obtained proper construct with omega-A fusion

Cloning of protein A DNA to OmpA constructs

  1. Colony PCR on colonies from plates with transformations pACYC177+OmpA_A_omega. Primers used: AL+SacI and AP+NotI
  2. Confirmed transformant colonies inoculated to liquid LB with kanamycin.
  3. Isolation of plasmids from cultures inocluated on previous day (pACYC177+OmpA_A_alpha).
  4. Control digest of isolated plasmids with BamHI and SacI.

Cloning of protein Z DNA to pET15b-OmpA-omega in place of OmpA
Paweł

  1. Ligations transformed into TOP10 and plated on LB + ampicillin.

Cloning omega-A fusion on pKS (second attempt)

Michał L., Ewa, Marcin:

  1. We have obtained white colonies of transformants and inoculated 10 of them on liquid LB+Amp100