Team:Newcastle/Labwork/24 September 2009

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(Difference between revisions)
(Formal Lab Session - 24th September 2009)
(Introduction)
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===Introduction===
===Introduction===
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[[Image:Team Newcastle 2009 iGEM 24-09-09 IMG 1373.JPG|200px|right]]
* We prepared kinA and pGFP-rrnB digested fragments yesterday, we'll carry on the next step as gel extraction and ligation and transformation.
* We prepared kinA and pGFP-rrnB digested fragments yesterday, we'll carry on the next step as gel extraction and ligation and transformation.
* For the double clone part, we need to ligate it to pMutin4 vector.
* For the double clone part, we need to ligate it to pMutin4 vector.

Revision as of 15:48, 21 October 2009


Team Newcastle 2009 iGEM ProbationaryP-Sign.PNG

Formal Lab Session - 24th September 2009

Team Newcastle 2009 iGEM 24-09-09 IMG 1379.JPG


Overview




Stochastic Switch Team

Today we did minipreps of the ara/sspb/pSB1AT3 cultures which were then digested with EcoRI and SpeI. These were run on an 0.8% gel. We expected to see a ~600bp band as well as the plasmid backbone and the gel photograph seemed fairly convincing:

Team Newcastle240909 trans mini.png

We set up a 50ml midiprep culture from the culture corresponding to lane 9 which seemed to have the clearest band.

Sporulation Tuning/Chassis Team

Introduction

Team Newcastle 2009 iGEM 24-09-09 IMG 1373.JPG
  • We prepared kinA and pGFP-rrnB digested fragments yesterday, we'll carry on the next step as gel extraction and ligation and transformation.
  • For the double clone part, we need to ligate it to pMutin4 vector.


Experiment procedure

Gel extraction

  • Follow the standard procedure of Gel Extraction Kit(Sigma).

Ligation

  • Ligate kinA to pGFP-rrnB
  • Ligate digested PCR clean-up psc fragment to pMutin4
    • this psc fragment refer to the cwlJ:sleB fragment with HindIII and BamHI restriction sites at the end of each side.
 T4 ligase Buffer        2ul
 Vector                2.5ul
 insert DNA           14.5ul
 T4 ligase               1ul
 ---------------------------
                        20ul
  • -4C frige overnight.

Prepare the culture for Mini Prep

  • Since we got colonies from yesterday's transformation, we need to culture the colonies for mini prep.

Prepare smm medium

  • The protocal of making smm medium is come from our lab's B.subtilis 168 transformation protocal.

Conclusion

  • After the autoclave of smm medium, the medium got cloudy. It may has something wrong with the ingredients.
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