Team:TUDelft/24 September 2009

From 2009.igem.org

(Difference between revisions)
(New page: {{Template:TUDelftiGEM2009}} {{Template:TUDelftiGEM2009_LabNotebook}} ='''24 September 2009'''= {{Template:TUDelftiGEM2009_end}})
(24 September 2009)
 
Line 4: Line 4:
='''24 September 2009'''=
='''24 September 2009'''=
-
 
+
We got sequencing results. It was found that the medium control RBS, Normal control RBS, LacI generator sequencing failed. But the locks and keys and negative cascade plasmids were partially confirmed. The Riboregulator plasmids has sequence similarity but not fully correct. Hence we think it is good to drop Riboregulator since we have no time to correct its assembly in which time we can concentrate on characterising the negative cascade plasmids.
-
 
+
Today I prepared the culture for miniprep of the LacI generator ligated negative cascade plasmid, riboregulator plasmid and locks and keys. Also I prepared some extra samples for sequencing. Also I prepared cultures for miniprep tomorrow for samples which has to be given for sequencing again (medium control RBS, Normal control RBS, LacI generator) and for reverse primer sequencing.
{{Template:TUDelftiGEM2009_end}}
{{Template:TUDelftiGEM2009_end}}

Latest revision as of 01:14, 22 October 2009

Lab Notebook

July
MTWTFSS
    1 2 3 4 5
6 7 8 9 10 11 12
13 14 15 16 17 18 19
20 21 22 23 24 25 26
27 28 29 30 31
August
MTWTFSS
          1 2
3 4 5 6 7 8 9
10 11 12 13 14 15 16
17 18 19 20 21 22 23
24 25 26 27 28 29 30
31
September
MTWTFSS
  1 2 3 4 5 6
7 8 9 10 11 12 13
14 15 16 17 18 19 20
21 22 23 24 25 26 27
28 29 30
October
MTWTFSS
      1 2 3 4
5 6 7 8 9 10 11
12 13 14 15 16 17 18
19 20 21 22 23 24 25
26 27 28 29 30 31
 

24 September 2009

We got sequencing results. It was found that the medium control RBS, Normal control RBS, LacI generator sequencing failed. But the locks and keys and negative cascade plasmids were partially confirmed. The Riboregulator plasmids has sequence similarity but not fully correct. Hence we think it is good to drop Riboregulator since we have no time to correct its assembly in which time we can concentrate on characterising the negative cascade plasmids. Today I prepared the culture for miniprep of the LacI generator ligated negative cascade plasmid, riboregulator plasmid and locks and keys. Also I prepared some extra samples for sequencing. Also I prepared cultures for miniprep tomorrow for samples which has to be given for sequencing again (medium control RBS, Normal control RBS, LacI generator) and for reverse primer sequencing.