Team:Newcastle/Labwork/29 September 2009

From 2009.igem.org

(Difference between revisions)
(Formal Lab Session - 29th September 2009)
(Chassis team)
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===Introduction===
===Introduction===
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* Two transformations need to be done today, one for psc-pMutin4 and another for kinA-pGFP-rrnB
-
 
+
-
 
+
<br>
<br>
===Experiment procedure===
===Experiment procedure===
-
==== 1 ====
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==== Transformation for E.coli ====
-
==== 2====
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* Followed Phil's protocal.
-
 
+
-
==== 3 ====
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 +
==== Digest the Mini Prep result for smtA:pMutin4 transformation====
 +
* This transformation was carried out by Matt and Arun.
 +
* HindIII and BamHI were used for digestion.
 +
  dd H2O                    7ul
 +
  10X fast digest buffer    2ul
 +
  Fast BamHI              0.5ul
 +
  Fast HindIII            0.5ul
 +
  Mini Prep DNA            10ul
 +
  ------------------------------
 +
                            20ul
 +
* 37C 1 hour.
 +
* Run the sample on 0.8% agarose gel.
===Conclusion===
===Conclusion===
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+
* After the digestion of smtA:pMutin4 Mini result, the 12 strains are not the right clone.
<br>
<br>
[[Image:|400px|center]]
[[Image:|400px|center]]
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===Futher plan===
 

Revision as of 00:25, 21 October 2009


Team Newcastle 2009 iGEM ProbationaryP-Sign.PNG

Contents

Formal Lab Session - 29th September 2009

Today we did miniprep for the ten ON cultures. Run them on thel gel.

After the results we did a restriction digest with HindIII and BamHI to find out the right colony.

However we did not get good results and we could not find the right colony we were looking for.

Chassis team

Introduction

  • Two transformations need to be done today, one for psc-pMutin4 and another for kinA-pGFP-rrnB


Experiment procedure

Transformation for E.coli

  • Followed Phil's protocal.

Digest the Mini Prep result for smtA:pMutin4 transformation

  • This transformation was carried out by Matt and Arun.
  • HindIII and BamHI were used for digestion.
 dd H2O                     7ul
 10X fast digest buffer     2ul
 Fast BamHI               0.5ul
 Fast HindIII             0.5ul
 Mini Prep DNA             10ul
 ------------------------------
                           20ul
  • 37C 1 hour.
  • Run the sample on 0.8% agarose gel.

Conclusion

  • After the digestion of smtA:pMutin4 Mini result, the 12 strains are not the right clone.


[[Image:|400px|center]]


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