Team:TU Delft/12 July 2010 content

From 2010.igem.org

(Difference between revisions)
(Lab Work)
(Lab Work)
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To prepare for the fluorescence assay measurements the strains were grown in M9 minimal medium containing 0.4% glucose and ampicillin.  
To prepare for the fluorescence assay measurements the strains were grown in M9 minimal medium containing 0.4% glucose and ampicillin.  
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High copy number RBS characterizations are rarely indicative of RiPS in system operation plasmids, thus the fluorescence assays will also be performed with the biobricks on pSB3C5. In order to obtain sufficient BioBrick DNA the strains were grown in 250 mL LB-Amp, awaiting isolation and plasmid swapping.
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High copy number RBS characterizations are rarely indicative of RiPS in system operation plasmids, thus the fluorescence assays will also be performed with the biobricks on pSB3C5. In order to obtain sufficient BioBrick DNA the strains were grown in 250 mL LB-Amp, awaiting QIAGEN Midi kit plasmid isolation and plasmid swapping.

Revision as of 22:37, 12 July 2010

Lab Work

Characterization of Anderson RBS sequences

E.coli TOP 10 strains containing the following composite biobricks in pSB1A2 had been obtained:

BioBrick # Composed of:
[http://partsregistry.org/Part:BBa_K398050 K398050] J23100 + J61100 + I13401
[http://partsregistry.org/Part:BBa_K398051 K398051] J23100 + J61101 + I13401
[http://partsregistry.org/Part:BBa_K398052 K398052] J23100 + J61107 + I13401
[http://partsregistry.org/Part:BBa_K398053 K398053] J23100 + J61117 + I13401
[http://partsregistry.org/Part:BBa_K398054 K398054] J23100 + J61127 + I13401

To prepare for the fluorescence assay measurements the strains were grown in M9 minimal medium containing 0.4% glucose and ampicillin.

High copy number RBS characterizations are rarely indicative of RiPS in system operation plasmids, thus the fluorescence assays will also be performed with the biobricks on pSB3C5. In order to obtain sufficient BioBrick DNA the strains were grown in 250 mL LB-Amp, awaiting QIAGEN Midi kit plasmid isolation and plasmid swapping.