Team:Newcastle/Transformation of E. coli
From 2010.igem.org
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==Materials required== | ==Materials required== | ||
- | * | + | * ''E. coli'' DH5α (200 µl) |
* Appropriate vector DNA | * Appropriate vector DNA | ||
* Heat block | * Heat block | ||
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==Protocol== | ==Protocol== | ||
- | # Thaw a 200 µl aliquot | + | # Thaw a 200 µl aliquot of ''E. coli'' DH4α and add the transforming DNA (10 ng of vector DNA in 10 µl). |
# Incubate on ice for 30 minutes. | # Incubate on ice for 30 minutes. | ||
# Heat-shock the cells for 120 seconds at 42°C, and place on ice again for 3-4 minutes. | # Heat-shock the cells for 120 seconds at 42°C, and place on ice again for 3-4 minutes. |
Latest revision as of 14:37, 26 October 2010
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Transformation of E. coli
Materials required
- E. coli DH5α (200 µl)
- Appropriate vector DNA
- Heat block
- Bucket of ice
- Pipettes
- Eppendorf tubes
- 1.5% agar plate containing appropriate antibiotics
Protocol
- Thaw a 200 µl aliquot of E. coli DH4α and add the transforming DNA (10 ng of vector DNA in 10 µl).
- Incubate on ice for 30 minutes.
- Heat-shock the cells for 120 seconds at 42°C, and place on ice again for 3-4 minutes.
- Add 1 ml of LB broth and incubate the cells at 37°C for 1-1.5 hr in a water bath with gentle shaking.
- Plate 200 µl of transformed E. coli onto 1.5% agar plate containing the appropriate selection markers.
- Incubate the plates overnight at 37°C.
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