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Team:TUDelft/21 August 2009
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| + | ===Calin=== | ||
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| + | Did colony PCR with Taq on 4 R751_oriTR_KO colonies and 2 R751_trbK_KO colonies. | ||
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| + | Mix shotgun sequencing mixes: | ||
| + | CA 1223 bp: A_VF, A_VR | ||
| + | CB 1162 bp: B_VF, B_VR | ||
| + | CC 311 bp: C_VF, C_VR | ||
| + | CE 231 bp: E_VF, E_VR | ||
{{Template:TUDelftiGEM2009_end}} | {{Template:TUDelftiGEM2009_end}} | ||
Revision as of 12:37, 19 October 2009
Lab Notebook
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21 August 2009
Saeed
!Fr1n downsteam was cut out agarose gel of 19-08-2009 and extracted by gel extraction kit. After extraction DNA concentration was 3.7 ng/microL. !C was digested by SpeI and PstI and !Fr1n downsteam is ligated into this. This construct is called !Z. After ligation !Z was transformed into electrocompetent cells and grown outside the incubator during weekend.
Tim Weenink
Calin
Did colony PCR with Taq on 4 R751_oriTR_KO colonies and 2 R751_trbK_KO colonies.
Mix shotgun sequencing mixes: CA 1223 bp: A_VF, A_VR CB 1162 bp: B_VF, B_VR CC 311 bp: C_VF, C_VR CE 231 bp: E_VF, E_VR
