Team:Austin Texas/interlab study

From 2014.igem.org

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=Devices Measured=
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*BBa_J23101 (constitive promoter) + BBa_E0240 (B0032 - RBS, E0040 - GFP, B0015 - double terminator) in pSB1C3
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*BBa_J23101 (constitive promoter) + BBa_E0240 (B0032 - RBS, E0040 - GFP, B0015 - double terminator) in pSBK3
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*BBa_J23115 (constitive promoter) + BBa_E0240 (B0032 - RBS, E0040 - GFP, B0015 - double terminator) in pSB1C3
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=Protocols=
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==Sample Preparation==
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*Inoculate 10 mL of LB with frozen stocks of the three transformed clones (I20260, J23101+E0240, J23115+E0240), a cell background control (TOP10 electrocompetent cells), and an LB only control in a 50 mL Erlenmeyer flask. Grow for 16-18 hours at 37°C, shaking at 300rpm.
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*The next morning, add 10µL of each overnight culture to 10 mL of LB with three replicates of each (15 total flasks) and grow 16-18 hours at 37°C, shaking at 300rpm.
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*Add 80 µL of each culture to the wells of a clear-bottomed black 96-well plate.
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==Measurement Protocol==
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*The samples were plated on a 96-well plate as follows:
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*
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*The 96-well plate was inserted into the Infinite 200 PRO Microplate Reader
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*Open Tecan i-control, the software used to document the readings
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*Configure the settings as detailed above
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*Obtain fluorescence and OD600 readings
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=Sequencing Data=

Revision as of 04:31, 10 October 2014