Imperial College/4 September 2008
From 2008.igem.org
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*GFP-Termiantor biobrick cut again with ''XbaI'' and ''SpeI'' to produce biobrick vectors for our PCR clones | *GFP-Termiantor biobrick cut again with ''XbaI'' and ''SpeI'' to produce biobrick vectors for our PCR clones | ||
*GFP-Termiantor biobrick cut again with ''EcoRI'' and ''SpeI'' to produce biobrick vectors for our GeneArt produced clones | *GFP-Termiantor biobrick cut again with ''EcoRI'' and ''SpeI'' to produce biobrick vectors for our GeneArt produced clones | ||
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====Results==== | ====Results==== | ||
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As can be seen, both the AmyE 3' integration sequence and the Aad9 (spectinomycin resistance) gene amplified properly. However, LacI did not and therefore, needs to be repeated. | As can be seen, both the AmyE 3' integration sequence and the Aad9 (spectinomycin resistance) gene amplified properly. However, LacI did not and therefore, needs to be repeated. | ||
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+ | ===Preparation of Electrocompetent ''E. coli'' Cells=== | ||
+ | We have prepared 42 aliquots of electrocompetent XL1 Blue ''E. coli'' cells using [http://openwetware.org/wiki/IGEM:IMPERIAL/2008/New/Protocols/XL1-Blue_preparation the relevant protocol] listed on our Protocols Page. The protocol was updated to include a higher innoculation value from the overnight culture. | ||
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==Dry Lab== | ==Dry Lab== |
Revision as of 23:06, 7 September 2008
4 September 2008WetlabCloning
ResultsAs can be seen, both the AmyE 3' integration sequence and the Aad9 (spectinomycin resistance) gene amplified properly. However, LacI did not and therefore, needs to be repeated.
Preparation of Electrocompetent E. coli CellsWe have prepared 42 aliquots of electrocompetent XL1 Blue E. coli cells using [http://openwetware.org/wiki/IGEM:IMPERIAL/2008/New/Protocols/XL1-Blue_preparation the relevant protocol] listed on our Protocols Page. The protocol was updated to include a higher innoculation value from the overnight culture.
Dry LabMotility
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