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12/07/13
From 2013.igem.org
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AliceHaworth (Talk | contribs) |
AliceHaworth (Talk | contribs) (→Transformation of RFP control plasmid) |
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***Positive control (normal plate) | ***Positive control (normal plate) | ||
***Negative control (No plasmid) | ***Negative control (No plasmid) | ||
| - | ***20ul of | + | ***20ul of 50pg/ul |
| - | ***200ul of | + | ***200ul of 50pg/ul |
***20ul of 10pg/ul | ***20ul of 10pg/ul | ||
***200ul of 10pg/ul | ***200ul of 10pg/ul | ||
*leave plates on bench overnight | *leave plates on bench overnight | ||
Latest revision as of 10:23, 14 August 2013
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Transformation of RFP control plasmid
- Keep competent cells on ice
- Add 50ul of cells to 4 tubes
- Add 1ul of resuspended DNA to 2 tubes
- Add 1ul RFP to the other 2 tubes
- Incubate for 30mins
- Heat shock at 42 degrees for 60secs
- Incubate on ice for 5mins
- Add 200ul of SOC media
- Incubate at 37degrees for 2hrs
- Spread on 6 plates:
- Positive control (normal plate)
- Negative control (No plasmid)
- 20ul of 50pg/ul
- 200ul of 50pg/ul
- 20ul of 10pg/ul
- 200ul of 10pg/ul
- leave plates on bench overnight
