Team:Newcastle/27 July 2010

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(Preparation for cloning of the rocF BioBrick)
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=Preparation for cloning of the rocF BioBrick=
=Preparation for cloning of the rocF BioBrick=
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Yesterday, we transformed ''E. coli'' DH5α with pSB1C3 and pSB1AK3. After checking the plates today for colonies we observed lots of pink colonies on the pSB1C3 plates and numerous white colonies on the pSB1AK3 plates.
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===Results===
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Yesterday, we transformed ''E. coli'' DH5α with pSB1C3 and pSB1AK3. After checking the plates today for colonies we observed lots of pink colonies on the pSB1C3 plates and numerous white colonies on the pSB1AK3 plates. Plates were then stored at 4°C as colonies will be used for minipreps.
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{{Team:Newcastle/footer}}

Revision as of 22:09, 27 October 2010

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Contents

Genomic DNA extraction experiment

Newcastle alan chromosome.jpg
Newcastle ice chromosome.jpg

Aims

The aim of today's experiment is to extract genomic DNA from both B. subtilis strains 168 and 3610. The genes necessary for the swarming BioBrick and rocF BioBrick will then hopefully be obtained from the genomic DNA using PCR.

Protocol

Discussion

At the end of the DNA precipitation step, we observed a small white pellet in all the eppendorf tubes.

Conclusion

The experiment was a success! The quality of the extracted DNA will be checked by using PCR on 28th July, 2010.

Preparation for cloning of the rocF BioBrick

Results

Yesterday, we transformed E. coli DH5α with pSB1C3 and pSB1AK3. After checking the plates today for colonies we observed lots of pink colonies on the pSB1C3 plates and numerous white colonies on the pSB1AK3 plates. Plates were then stored at 4°C as colonies will be used for minipreps.

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