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+ | <h2 class="left"><a href = "https://2016.igem.org/Team:CSU_Fort_Collins/NoteBook/July"> << July</a> | ||
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+ | <h2 class="right"><a href = "https://2016.igem.org/Team:CSU_Fort_Collins/NoteBook/Sep">September >></h2> | ||
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</html> | </html> |
Revision as of 22:48, 17 October 2016
August
8/5/16:
- Phosphorylated Qblocks and pSB1C3
- Performed ligase cycling on phosphorylated mixture, but instead used an annealing temperature of 55C
- Gel had no bands
8/6/16:
- Performed Colony PCR on Slr0118+Luc transformed colonies
- Ran PCR results on a 1% gel
- Gel had no bands
8/8/16:
- Digested I712013 and Luc
- Ligated I712013 and Luc
- Transformed ligation mixture
8/9/16:
- PCRed out T7 polymerase N and C from T7 polymerase
8/11/16:
- Colony PCRed transformed 21 I7+Luc colonies
8/12/16:
- Phosphorylated Q1 and Q2 for ligase cycling
8/15/16:
- Performed ligase cycling reaction on phosphorylated Q block mixture
8/19/16:
- Performed colony PCR on Slr0168+Luc
8/23/16:
- Performed colony PCR on Slr0168+Luc and Quorum block
- Transformed Slr0168+Luc ligation mixture
- Performed 2-step PCR on Q1 and Q2
- RePCRed Q1,Q2,and pSB1C3 for ligase cycling
8/25/16:
- Digested Slr0168(ECORI PstI) and Luc(ECORI PstI)
- Ligated Slr0168 and Luc overnight at 16C
8/26/16:
- Ran PCR products from the 23rd on a 1.5% gel
8/30/16:
- Slr0168+Luc and Qblock transformed colonies were colony PCRed with Q5 master mix
- Slr0168+Luc colonies apear to have worked