Team:Warsaw/Calendar-Main/27 May 2008

From 2008.igem.org

(Difference between revisions)
Line 9: Line 9:
<p>2. <a href:"https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#plasmid_DNA_isolation">Isolation</a> of hypothetical pMPM-T5 with translation fusion.</p>
<p>2. <a href:"https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#plasmid_DNA_isolation">Isolation</a> of hypothetical pMPM-T5 with translation fusion.</p>
-
<p>3. Control <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#digest">digestion</a> of pMPM-T5 with transcription fusion with EcoRI and XhoI (2x Tango buffer).</p>
+
<p>3. Control <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#digest">digest</a> of pMPM-T5 with transcription fusion with EcoRI and XhoI (2x Tango buffer).</p>
-
<p>4. Control <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#digest">digestion</a> of pMPM-T5 with translation fusion with BamHI (BamHI buffer).</p>
+
<p>4. 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).</p>
-
<p>5. Control <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#digest">digestion</a> of pMPM-T5 with translation fusion with EcoRI and XbaI (2x Tango buffer).</p>
+
<p>5. 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 EcoRI and XbaI (2x Tango buffer).</p>
<p>6. Choice of proper clones and preparation for sequencing.</p>
<p>6. Choice of proper clones and preparation for sequencing.</p>

Revision as of 17:52, 1 October 2008

Gallery Bricks Notebook Team Project Home


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

 


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 and XhoI (2x Tango buffer).

4. Control digest of pMPM-T5 with translation fusion with BamHI (BamHI buffer).

5. Control digest of pMPM-T5 with translation fusion with EcoRI and XbaI (2x Tango buffer).

6. Choice of proper clones and preparation for sequencing.

Here we found the clone with translational fusion on pMPM. These are different isolations in each lane. We have been working with the AT6 ever since.
Digestion was conducted with BamHI

Trawienie_06_05_2008.jpg