Team:UNICAMP-Brazil/Notebooks/August 18

From 2009.igem.org

(Difference between revisions)
(YeastGuard)
(ColiGuard)
 
(One intermediate revision not shown)
Line 8: Line 8:
====Terminator biobrick====
====Terminator biobrick====
-
*<p style=”text-align:justify;”>
+
*<p style=”text-align:justify;”>The biobrick BBa_J63002 was ressuspended from the plate and the transformed ''E. coli'' have occupied the whole plates, both LB-AMP and LB-KAN plates. We decided to replicate these colonies in other plates in order to get isolated colonies for the miniprep.</p>
-
The biobrick BBa_J63002 was ressuspended from the plate and the transformed ''E. coli'' have occupied the whole plates, both LB-AMP and LB-KAN plates. We decided to replicate these colonies in other plates in order to get isolated colonies for the miniprep.</p>
+
''Taís''
''Taís''
Line 17: Line 16:
====Enzyme restriction====
====Enzyme restriction====
-
We made the Mini-prep (according to the protocol 2) and immediately make enzyme restriction with XbaI e PstI in order to prove the part existing in the plasmids. We didn’t find the correct band size (514 bp); we just found the linear plasmid size band.
+
*<p style=”text-align:justify;”>We performed miniprep according to [https://2009.igem.org/Team:UNICAMP-Brazil/Protocols/Mini-Prep Protocol 2] and immediately made enzymatic digestion using ''Xba''I and ''Pst''I in order to prove the existing part in the plasmids. We didn’t find the correct band size (514 bp); we just found the linear plasmid size band.</p>
[[Image:18_agosto.jpg‎‎ |center|‎]]
[[Image:18_agosto.jpg‎‎ |center|‎]]

Latest revision as of 01:06, 22 October 2009

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

YeastGuard

Terminator biobrick

  • The biobrick BBa_J63002 was ressuspended from the plate and the transformed E. coli have occupied the whole plates, both LB-AMP and LB-KAN plates. We decided to replicate these colonies in other plates in order to get isolated colonies for the miniprep.

Taís

ColiGuard

Enzyme restriction

  • We performed miniprep according to Protocol 2 and immediately made enzymatic digestion using XbaI and PstI in order to prove the existing part in the plasmids. We didn’t find the correct band size (514 bp); we just found the linear plasmid size band.

‎

Luige