Team:Warsaw/Calendar-Main/22 May 2008

From 2008.igem.org

(Difference between revisions)
Line 27: Line 27:
<li> Control <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#digest">digest</a> of pMPM-T5 with translation fusion with BamHI (BamHI buffer).</li>
<li> Control <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#digest">digest</a> of pMPM-T5 with translation fusion with BamHI (BamHI buffer).</li>
-
<li> Gel electrophoresis (no proper colonies found).</li></html>
+
<li> Gel electrophoresis (no proper colonies found).</li>
 +
<img src="https://static.igem.org/mediawiki/2008/8/87/Aid_fusion_digests_WAW.jpg"width=300/>
 +
<h3>1-DNA ladder; 2 and 3-hypothetical pMPM-T5 with transcription fusion digested with EcoRI (2 clones); 4-pMPM-T5-AID  digested with EcoRI; 5-hypothetical pMPM with translation fusion digested with BamHI; 6-pMPM-T5-AID digested with BamHI.</h3>
 +
</html>
<!-- do not remove this! -->
<!-- do not remove this! -->
{{WarNotebookEnd}}
{{WarNotebookEnd}}

Revision as of 08:08, 6 October 2008

Gallery Bricks Notebook Team Project Home


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

 


Preparation of pMPMT5-AID+T7 and pMPMT5+AID-T7

Piotr:

  1. Design of primers for sequencing something we want from pMPM-T5.

  2. Primers:

Michał K.:

  1. Isolation of hypothetical pMPM-T5 with transcription fusion.
  2. Isolation of hypothetical pMPM-T5 with translation fusion.
  3. Control digest of pMPM-T5 with transcription fusion with EcoRI (EcoRI buffer).
  4. Control digest of pMPM-T5 with translation fusion with BamHI (BamHI buffer).
  5. Gel electrophoresis (no proper colonies found).
  6. 1-DNA ladder; 2 and 3-hypothetical pMPM-T5 with transcription fusion digested with EcoRI (2 clones); 4-pMPM-T5-AID digested with EcoRI; 5-hypothetical pMPM with translation fusion digested with BamHI; 6-pMPM-T5-AID digested with BamHI.