2014hs.igem.org/team:Charlottesville RS/Notebook/032814
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== March 28th, 2014 == | == March 28th, 2014 == | ||
+ | ''Jessica Prax, John Grammer, Nick Keen, Alli Ambrosini'' | ||
+ | |||
+ | Ligation: | ||
+ | |||
+ | Jess and John: Added 1 microliter of T4 DNA ligase instead of 5 microliters. The rest of the procedure is the same as Nick and Allis’ procedure, but with IGEM’s parts A and B, and plus the ligation control steps (look at IGEM packet page 18 steps 3, 4 and 5) | ||
+ | |||
+ | Nick and Alli: Performed the same procedure as Jess and John, without the Ligation control and with the parts A and B that were made before. | ||
+ | - The mixture was pSB1C3, the Part A and Part B that were made at the Renaissance Lab, T4 Dna Ligase, and T4 ligase reaction buffer. | ||
+ | - Incubated this mixture at 16 degrees Celsius for 30 minutes, then at 80 degrees Celsius for 20 minutes. | ||
+ | |||
+ | [[https://2014hs.igem.org/Team:Charlottesville_RS/Notebook/Overview Back]] |
Latest revision as of 13:56, 20 June 2014
March 28th, 2014
Jessica Prax, John Grammer, Nick Keen, Alli Ambrosini
Ligation:
Jess and John: Added 1 microliter of T4 DNA ligase instead of 5 microliters. The rest of the procedure is the same as Nick and Allis’ procedure, but with IGEM’s parts A and B, and plus the ligation control steps (look at IGEM packet page 18 steps 3, 4 and 5)
Nick and Alli: Performed the same procedure as Jess and John, without the Ligation control and with the parts A and B that were made before. - The mixture was pSB1C3, the Part A and Part B that were made at the Renaissance Lab, T4 Dna Ligase, and T4 ligase reaction buffer. - Incubated this mixture at 16 degrees Celsius for 30 minutes, then at 80 degrees Celsius for 20 minutes.
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