Team:Aberdeen Scotland/notebook/andgate
From 2009.igem.org
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*End of week meeting to present weeks work and plan ahead | *End of week meeting to present weeks work and plan ahead | ||
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- | ==Week 3: Edinburgh iGEM meeting and | + | ==Week 3: Edinburgh iGEM meeting and Digestions(22/06/09 - 26/06/09)== |
===Day 1 Monday (22/06/09)=== | ===Day 1 Monday (22/06/09)=== | ||
- | *Preperation for cloning and selection of desired | + | *Preperation for cloning and selection of desired biobricks from earlier rescues |
<br><br> | <br><br> | ||
===Day 2 Tuesday (23/06/09)=== | ===Day 2 Tuesday (23/06/09)=== |
Revision as of 16:05, 12 August 2009
University of Aberdeen - Pico Plumber
iGEM 2009
AND Gate Notebook
Week 1: Research and Planning (08/06/09 - 12/06/09)
Day 1 Monday (08/06/09)
- Researching the Registry for Biobricks
- Focus on T7 parts (I712074, I719005, K113011, K113012, J34814, K103021, R0085, R0180, R0182, Z0251 and Z0252) for possible use in our project.
- Other BioBricks identified for other sub-projects include R0062, J40001, J37015 and R0063
Day 2 Tuesday (09/06/09)
- Researching literature for T7 promoter strength and degradation rate
- Useful article - Imburgio, D., Rong, M., Ma, K., and W. T. McAllister. (2000) "Studies of Promoter Recognition and Start Site Selection by T7 RNA Polymerase Using a Comprehensive Collection of Promoter Variants" Biochemistry.39:10419-10430
Day 3 Wednesday (10/06/09)
- Researching literature for parameters of LuxR, LacO, TetO and cIO
- Useful article - Braff, J. C., Conboy, C. C., and D.E. Endy. Promoter Characterization Experiments. (found at openwetware.org/images/3/30/PromoterChar_Report_Revised.doc)
- Identified plasmids that potential Biobricks were on and prepared for rescue.
- Also indentified LVA tags and any other anomalies on selected Biobricks.
Day 4 Thursday (11/06/09)
- PoPs to LacZ alpha repoter identified (E0435) and potenially useful Input Output sensor (pSB1A10)
- Other possible reporters include LacZ alpha fragments and Enhanced stable YFP.
- Possibility of intentional SNP generated within T7 to alter promoter strength was deemed unworkable in the scale of project.
Day 5 Friday (12/06/09)
- End of week meeting
- Discussion and planning for following week
Week 2: BioBrick Rescue (15/06/09 - 19/06/09)
Day 1 Monday (15/06/09)
- Prepared LB medium and LB+Amp plates
- Preperation of Kanamycin stock (30mg ml-1)
- Inoculated C0040, R0062, J37033 and C0051 for miniprep the following day
Day 2 Tuesday (16/06/09)
- Miniprep of above Biobricks
- Restriction digest of C0040, R0062, J37033 and C0051 with EcoRI-HF + SpeI and gel electrophoreis of these.
Day 3 Wednesday (17/06/09)
- Rescue of a range of vectors (pSB1AT3, pSB1AC3, pSB3T5, pSB3C5, pSB4T5, pSB4C5)
- Preperation of Tet and Chlo agar plates for the above
- Transformation of DB3.1 cells (ccdB gene resistant)
Day 4 Thursday (18/06/09)
- Preparation of more Chlo and Tet plates.
- Sub-cultivation of transformants
Day 5 Friday (19/06/09)
- End of week meeting to present weeks work and plan ahead
Week 3: Edinburgh iGEM meeting and Digestions(22/06/09 - 26/06/09)
Day 1 Monday (22/06/09)
- Preperation for cloning and selection of desired biobricks from earlier rescues
Day 2 Tuesday (23/06/09)
- Edinburgh Igem Meeting
Day 3 Wednesday (24/06/09)
- Edinburgh Igem Meeting
Day 4 Thursday (25/06/09)
- Double digest of the biobricks B0030, C0051, I0462, J23105, J23107, J23115, with EcoRI-HF + Spe I
- Double digest of the biobricks S03518, E0840 with XbaI + PstI
- Double digest of the biobricks pSB3K3, pSB4K5, pSB3T5, pSB1AC3, pSB1AT3
Day 5 Friday (26/06/09)
- DB3.1 cells transformed with pSB1AK3
- Gel Electrophoresis of above digests
- End of week meeting
Week 4 29/06/09 - 03/07/09
Week 5 05/07/09 - 10/07/09
Week 6 13/07/09 - 16/07/09
Week 7 20/07/09 - 24/07/09
Week 8 27/07/09 - 31/07/09
Week 9 03/08/09 - 07/08/09
Week 10 10/08/09 - 14/08/09
Week 11 17/08/09 - 21/08/09
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