Team:UNICAMP-Brazil/Notebooks/October 14

From 2009.igem.org

(Difference between revisions)
(YeastGuard)
(New strategy: pGEM)
Line 10: Line 10:
*<p style=”text-align:justify;”>We did miniprep of 10 Adh1+Lysozyme colonies.</p>
*<p style=”text-align:justify;”>We did miniprep of 10 Adh1+Lysozyme colonies.</p>
-
*<p style=”text-align:justify;”>We digested the Adh1+Lysozyme/biofusion minipreps in order to connect it to the yeast expression vector (YEP). We used the ''Xba''I and ''Pst''I enzymes. 9 of 10 digestions worked! =) The expected fragment size is 2000bp.</p>
+
*<p style=”text-align:justify;”>We digested the Adh1+Lysozyme/biofusion minipreps in order to connect it to the yeast expression vector (YEP358). We used the ''Xba''I and ''Pst''I enzymes. 9 of 10 digestions worked! =) The expected fragment size is 2000bp.</p>
[[Image:adh1+lis.jpg|500px|center]]
[[Image:adh1+lis.jpg|500px|center]]
   
   
-
*<p style=”text-align:justify;”>We chose two fragments and purified them from the agarose gel. We ligated them to YEP. We will transform it tomorrow.</p>
+
*<p style=”text-align:justify;”>We chose two fragments and purified them from the agarose gel. We ligated them to YEP358. We will transform it tomorrow.</p>

Revision as of 18:42, 21 October 2009

Topo l2.gif topo_r_igem.gif
topo_r_b.gif
Back to Calendar

YeastGuard

New strategy: pGEM

  • We did miniprep of 10 Adh1+Lysozyme colonies.

  • We digested the Adh1+Lysozyme/biofusion minipreps in order to connect it to the yeast expression vector (YEP358). We used the XbaI and PstI enzymes. 9 of 10 digestions worked! =) The expected fragment size is 2000bp.

Adh1+lis.jpg
  • We chose two fragments and purified them from the agarose gel. We ligated them to YEP358. We will transform it tomorrow.


Raíssa and Taís