IGEM:Arizona State/2014/Notebook/asu igem 2014/2014/07/15: Difference between revisions

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*After ligation, the mixture was heated to 65°C for 10 min. to denature the ligaze.
*After ligation, the mixture was heated to 65°C for 10 min. to denature the ligaze.
*Transformation was then performed.
*Transformation was then performed.
:Three plates were grown overnight: RBS backbone (vector), TesA+RBS, and mCherryboth as a positive control and to replenish our stocks.


* Transformation
* Transformation
:Unfortunately, no growth was seen on any of the plates, including the positive control of mCherry.


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Revision as of 07:46, 16 July 2014

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TesA/RBS Ligation Attempt 2

  • Checked DNA concentrations
TesA= 11.99 ng/μL ; RBS=32.99 ng/μL
  • When divided by the number of base pairs: [TesA]=.018 and [RBS]=.016
  • Ligation
Reagent (μL) Volume (μL)
DNA(plasmid) 1.0 μL RBS, 2.0 μL TesA
10X buffer 1.0
dH2O 5.0
Ligaze 1.0
  10.0 μL --> 25°C/ ~1 Hr.
  • After ligation, the mixture was heated to 65°C for 10 min. to denature the ligaze.
  • Transformation was then performed.
Three plates were grown overnight: RBS backbone (vector), TesA+RBS, and mCherryboth as a positive control and to replenish our stocks.
  • Transformation
Unfortunately, no growth was seen on any of the plates, including the positive control of mCherry.
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