User:University of Washington/9 July 2008

From 2008.igem.org

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== RP4 Conjugation ==
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·Success!!!  Bacteria-Bacteria conjugation works<br\>
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·Received lambda red primers for RP4 manipulation
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== LuxR from AraC and TetR ==
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- Took AraC plasmid after thermo cycling out from the machine, stored in the fridge.
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- Plated GFP generator (BBa_E0240: received from BioCircuit Lab) on LB Agar + Amp.
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== BioBrick Promoter Measurements ==
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- Overnight promoter-construct cultures were diluted 1:100, then incubated in a rotator for 3 hours.
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- Using a 96-well plate reader, fluorescence and OD600 measurements were taken every five minutes for eight hours for the four promoter-construct cultures, an empty culture of TOP10 cells, M9 media, and M9+Kan.
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==LuxR from pLac==
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-Part I736004 sequence was confirmed.
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-Overnight culture of I736004 transformed cells were started in M9 media.
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Back to [[Team:University_of_Washington/Notebook#Notebook]]
Back to [[Team:University_of_Washington/Notebook#Notebook]]

Latest revision as of 23:40, 24 July 2008

Contents

RP4 Conjugation

·Success!!! Bacteria-Bacteria conjugation works
·Received lambda red primers for RP4 manipulation

LuxR from AraC and TetR

- Took AraC plasmid after thermo cycling out from the machine, stored in the fridge.

- Plated GFP generator (BBa_E0240: received from BioCircuit Lab) on LB Agar + Amp.

BioBrick Promoter Measurements

- Overnight promoter-construct cultures were diluted 1:100, then incubated in a rotator for 3 hours.

- Using a 96-well plate reader, fluorescence and OD600 measurements were taken every five minutes for eight hours for the four promoter-construct cultures, an empty culture of TOP10 cells, M9 media, and M9+Kan.

LuxR from pLac

-Part I736004 sequence was confirmed.

-Overnight culture of I736004 transformed cells were started in M9 media.



Back to Team:University_of_Washington/Notebook#Notebook