Team:UC Davis/Notebook wip
From 2011.igem.org
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+ | == Week 1== | ||
+ | -Rehydrated parts from 2011 Registry Distribution: | ||
+ | **-R0040=Tet promoter in psb1a2 | ||
+ | **-C0040=Tet repressor in psb1a2 | ||
+ | **-C0012=LacI repressor in psb1a2 | ||
+ | **-C0051=Lambda cI repressor in psb1a2 | ||
+ | **-R0051=cI-regulated promoter in psb1a2 | ||
+ | **-I732006=LacZ-alpha in psb1ak3 | ||
+ | **-R0010=LacI regulated promoter in psb1a2 | ||
+ | **-E0040=GFP coding region in psb1a2 | ||
+ | **-J23101=Constitutive promoter in j61002 | ||
+ | **-C0080=AraC repressor/activator in psb2k3 | ||
+ | **-I13458=pC+AraC in psb1a3 | ||
+ | **-I13453=pBAD promoter in psb1a3 | ||
+ | **-B0015=Double terminator in psb1ak3 | ||
+ | -Transformed all hydrated parts | ||
+ | -Cultured all parts and digested to check on a gel. All parts checked out. Sent out all hydrated parts to get sequenced. | ||
+ | -Ligated mutants into screening plasmid to see if our error-prone PCRs had visible mutants. | ||
+ | -Ordered primers for mutagenesis of LacI promoter, cI promoter and tet promoter. Also ordered primers to replace RBS (Bba_B0032) in Bba_E0240 to Bba_B0034. | ||
+ | |||
+ | == Week 2== | ||
+ | == Week 3 == | ||
+ | == Week 4 == | ||
+ | == Week 5 == | ||
+ | == Week 6 == | ||
+ | == Week 7 == | ||
+ | == Week 8 == | ||
+ | == Week 9 == | ||
+ | == Week 10 == | ||
+ | |||
+ | </html> |
Revision as of 18:59, 24 June 2011
Start a Family
Got a favorite BioBrick? Check our our process for expanding basic parts into part families.Criteria
View our judging criteria for iGEM 2011 here.
== Week 1==
-Rehydrated parts from 2011 Registry Distribution:
**-R0040=Tet promoter in psb1a2
**-C0040=Tet repressor in psb1a2
**-C0012=LacI repressor in psb1a2
**-C0051=Lambda cI repressor in psb1a2
**-R0051=cI-regulated promoter in psb1a2
**-I732006=LacZ-alpha in psb1ak3
**-R0010=LacI regulated promoter in psb1a2
**-E0040=GFP coding region in psb1a2
**-J23101=Constitutive promoter in j61002
**-C0080=AraC repressor/activator in psb2k3
**-I13458=pC+AraC in psb1a3
**-I13453=pBAD promoter in psb1a3
**-B0015=Double terminator in psb1ak3
-Transformed all hydrated parts
-Cultured all parts and digested to check on a gel. All parts checked out. Sent out all hydrated parts to get sequenced.
-Ligated mutants into screening plasmid to see if our error-prone PCRs had visible mutants.
-Ordered primers for mutagenesis of LacI promoter, cI promoter and tet promoter. Also ordered primers to replace RBS (Bba_B0032) in Bba_E0240 to Bba_B0034.
== Week 2==
== Week 3 ==
== Week 4 ==
== Week 5 ==
== Week 6 ==
== Week 7 ==
== Week 8 ==
== Week 9 ==
== Week 10 ==