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05/09/13
From 2013.igem.org
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AliceHaworth (Talk | contribs) |
(→Transformation of pSB1C3/TOD genes) |
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The controls for this experiment are the resistance and viability controls. | The controls for this experiment are the resistance and viability controls. | ||
One tube has 50 ul of highly competent cells and SOC medium added to it. | One tube has 50 ul of highly competent cells and SOC medium added to it. | ||
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| + | The samples A (TodX), C (TodF), E(ToBG), positive control, and background control were plated on chlorophenicol resistant agar plates, at the volumes of 20ul and 200ul. A 100ul of only highly efficient cells and SOC medium was plated in a chlorophenicol plate and another 100ul was plated on a LB plate. | ||
==Isolate plasmid from overnight broth== | ==Isolate plasmid from overnight broth== | ||
==Double digest of isolated plasmid== | ==Double digest of isolated plasmid== | ||
Revision as of 08:50, 6 September 2013
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Transformation of pSB1C3/TOD genes
- Centrifuge the ligation
- Add 6 ul of each ligation reaction to a sterile 1.5ml tube on ice
- Thaw the cells on ice
- Carefully transfer 50ul of cells to the ligation reaction. Gently flick the tubes and incubate on ice for 20 minutes.
- Heat shock the cells for 45 seconds in a 42'C water bath. Do not shake. Immediately return the tubes to ice for 2 minutes.
- Add 950 ul of SOC medium (at room temperature) to the ligation reactions. Incubate for 1.5 hours at 37'C on a shaker.
The controls for this experiment are the resistance and viability controls. One tube has 50 ul of highly competent cells and SOC medium added to it.
The samples A (TodX), C (TodF), E(ToBG), positive control, and background control were plated on chlorophenicol resistant agar plates, at the volumes of 20ul and 200ul. A 100ul of only highly efficient cells and SOC medium was plated in a chlorophenicol plate and another 100ul was plated on a LB plate.
