Team:TUDelft/8 July 2009

From 2009.igem.org

(Difference between revisions)
 
Line 1: Line 1:
{{Template:TUDelftiGEM2009}}
{{Template:TUDelftiGEM2009}}
 +
 +
{{Template:TUDelftiGEM2009_LabNotebook}}
 +
='''8th July'''=
='''8th July'''=
<br>
<br>
=='''Conjugation'''==
=='''Conjugation'''==
Today, we worked on the entries to the Parts Registry, where we used some parts from the Peking '07 iGEM team and some parts from NCBI. After writing down the sequences for trbC (pilin) of IncP beta R751 plasmid, trbK (entry exclusion) of IncP beta R751 plasmid, I-PpoI homing endonuclease site, I-SceI homing endonuclease site and I-PpoI homing endonuclease into the registry, we used the software [http://www.vectorcore.pitt.edu/upgene/upgene.html Upgene] to optimize for the codons, and the optimized sequences were inserted into the Parts Registry.
Today, we worked on the entries to the Parts Registry, where we used some parts from the Peking '07 iGEM team and some parts from NCBI. After writing down the sequences for trbC (pilin) of IncP beta R751 plasmid, trbK (entry exclusion) of IncP beta R751 plasmid, I-PpoI homing endonuclease site, I-SceI homing endonuclease site and I-PpoI homing endonuclease into the registry, we used the software [http://www.vectorcore.pitt.edu/upgene/upgene.html Upgene] to optimize for the codons, and the optimized sequences were inserted into the Parts Registry.
 +
 +
{{Template:TUDelftiGEM2009_end}}
{{Template:TUDelftiGEM2009_end}}

Latest revision as of 14:27, 25 July 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
 

8th July


Conjugation

Today, we worked on the entries to the Parts Registry, where we used some parts from the Peking '07 iGEM team and some parts from NCBI. After writing down the sequences for trbC (pilin) of IncP beta R751 plasmid, trbK (entry exclusion) of IncP beta R751 plasmid, I-PpoI homing endonuclease site, I-SceI homing endonuclease site and I-PpoI homing endonuclease into the registry, we used the software [http://www.vectorcore.pitt.edu/upgene/upgene.html Upgene] to optimize for the codons, and the optimized sequences were inserted into the Parts Registry.