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Team:Arizona State/Notebook
From 2012.igem.org
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Rohit Rajan (Talk | contribs) (→August 13) |
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[[File: ASUiGEM2012_gel081312.jpeg|200px]] | [[File: ASUiGEM2012_gel081312.jpeg|200px]] | ||
| - | ==August | + | ==August 14== |
* Assembled magainin insert via Overlapping oligo assembly | * Assembled magainin insert via Overlapping oligo assembly | ||
* Digested pUC 19 plasmid with EcoRI and PstI | * Digested pUC 19 plasmid with EcoRI and PstI | ||
* Transformed Magainin insert into digested pUC 19 plasmid. Failed. Probably too much X-gal on plate. | * Transformed Magainin insert into digested pUC 19 plasmid. Failed. Probably too much X-gal on plate. | ||
| + | [[File: ASUiGEM2012_gel081412.jpeg|200px]] | ||
==August 15== | ==August 15== | ||
Revision as of 03:56, 3 October 2012
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Note from Dr. Haynes: Rohit, please transfer all of the Notebook entries from the OWW Wiki
http://openwetware.org/wiki/Haynes_Lab:Notebook/ASU_iGEM
To this page. Follow the format below. I added a couple of sections to help you get started.
June 07
- Transformation (LSE)
- Transformed DNA:
- lacZ (well 4:12G, I732019)
- p + lacO (well 1:6G, R0011)
- Cells: neb10beta (donated)
- Protocol from: http://www.neb.com/nebecomm/products/productc3019.asp
- Controls: puc19, no DNA (8 plates)
- Transformed DNA:
June 08
- Transformation results
- puc19: growth
- negative control: no growth
- lacZ, lacO: possible small colonies
- liquid culture in amp media (100 ug / ml):
- no growth of lacZ, lacO
- growth of puc19
June 12
- DH5a Competent Cell Prep
- Streak plated cells on LB no amp plate, let grow overnight
June 13
- Transformation (LSE)
- Transformed DNA:
- lacZ (well 4:12G, I732019)
- p + lacO (well 1:6G, R0011)
- Cells: DH5 alpha (donated)
- Protocol from: http://openwetware.org/wiki/Haynes:Assembly101 (30 minute transformation)
- Controls: puc19, no DNA (8 plates)
- Transformed DNA:
- Transformation (istb4, Abhi)
- Transformed DNA:
- Cells:
- Protocol from:
- Controls:
- DH5a Chemically Competent cell prep
- Grew 2 seed colonies from streak plate in LB no amp
- Grew controls to test for contamination
- Both Seed colonies grew, no contamination present
June 14
- Competent cell prep
- Prepared CaCl2 buffer solution and CaCl2 glycerol buffer solution
- Grew seed colony in 400mL LB no amp
June 15
- Competent cell prep
- Centrifuged falcon test tubes containing liquid colonies
- Resuspended in CaCl2 buffer solution and incubated for 15 mins
- Centrifuged and resuspended in CaCl2 glycerol buffer solution
- Chilled overnight
June 16
- Competent cell prep
- Aliquotted 200uL into test tubes
- Stored in -80C
June 17
- Streak plated prepared competent cells on LB no amp plate
- Colonies observed
June 19
- Transformation (LSE)
- Transformed DNA:
- T7 promoter BBa_I712074
- Constitutive promoter BBa_J23102
- Cells: DH5 alpha (donated)
- Protocol from: http://tools.invitrogen.com/content/sfs/manuals/subcloningefficiencydh5alpha_man.pdf (30 minute transformation)
- Controls: puc19, no DNA
- Plated 2 copies of each (100 ul, 250 ul) on LB amp plates.
- Transformed DNA:
- Made 50 LB Amp plates.
June 20
- Plated negative control on LB Amp plate
- Liquid cultures of T7 promoter and constitutive promoter
- Transformation (LSE)
- Transformed DNA:
- RBS (well 1:1H BBa_B0030)
- TetR GFP (well 2:8A Part:BBa_I13522)
- Cells: DH5 alpha (donated)
- Protocol from: http://tools.invitrogen.com/content/sfs/manuals/subcloningefficiencydh5alpha_man.pdf (30 minute transformation)
- Controls: puc19, no DNA
- Transformed DNA:
June 21
- Made Liquid Cultures of E.coli transformed with RBS B0030
- Made Liquid Cultures of E.coli transformed with TetR GFP
- miniprepped and nanodropped T7 promoter BBa_I712074 and Constitutive promoter BBa_J23102 liquid cultures
- liquid cultures:
- RBS1
- RBS2 (duplicate_
- GFP1
- puc19
- negative controls
- 5 ml LB amp
- overnight cultures
- replated GFP1 & 2 (duplicates)
- Nanodropped plasmid DNA samples
- Constitutive promoter 1: __ng/uL
- Constitutive promoter 2: __ng/uL
- T7 promoter 1: __ng/uL
- T7 promoter 2: __ng/uL
June 22
- Miniprepped liquid cultures: RBS (well 1:1H BBa_B0030) and TetR GFP (well 2:8A Part:BBa_I13522)
June 26
- Transformation:
- Transformed DNA:
- double terminator (B0017, 2:6K)
- T7 RNA polymerase (I715038, 2:15C)
- puc19, negative control
- Protocol from: http://tools.invitrogen.com/content/sfs/manuals/subcloningefficiencydh5alpha_man.pdf (30 minute transformation)
- Cells: dh5a
- Transformed DNA:
June 27
- 6-26 transformation results:
- Controls correct
- 2x terminator: ~19 colonies
- RNA pol: 1 colony
- Liquid cultures including controls
June 28
- Miniprepped double terminator (B0017, 2:6K) and T7 RNA polymerase (I715038, 2:15C) liquid cultures
July 2
- Cleaned up liquid waste
- Made SOB media
- Finalized oligos for magainin construct
July 3
- Autoclaved SOB media
- Added glucose to make SOC media
- Nanodropped double terminator (B0017, 2:6K) [DT1: 24.5, DT2: 29.6] and T7 RNA polymerase (I715038, 2:15C) [P1: 64.6, P2: 55.3] liquid cultures
July 24
- Plasmids arrived courtesy of University of Pennsylvania School of Medicine
- pET29a vectors containing coding sequence for Topoisomerase mutants CSCS and CSCS D168A described here
July 25
- Tranformed CSCS topo 0 plasmid and CSCS D168A topo into DH5a Turbo cells (with neg control and Puc19 neg control)
- Plated on Kanamycin plates
July 26
- Picked colonies colonies from Topo 0 and Topo D168A and grew liquid cultures in Kan media
July 27
- Miniprepped liquid colonies and nanodropped.
- Plasmid concentrations
- Topo O:
- Topo D168A1:
- Topo D168A2:
July 30
- Prepared Kan Media and Kan Plates
July 31
- PCR amplified polylinker sequence of Topo plasmid with Promega GoTaq protocol
- Used pET29a upstream forward primer and T7 terminator reverse primer
August 3
- Submitted pET29a Topoisomerase plasmid to Biodesign for sequencing
August 10
- PCR of Alpha-4, 1-omega, omega, and alpha fragments using corrected primers
August 13
- Ran gel of split beta gal fragments. Confirmed 3 out of the 4 fragments except for the alpha-4 fragment.
August 14
- Assembled magainin insert via Overlapping oligo assembly
- Digested pUC 19 plasmid with EcoRI and PstI
- Transformed Magainin insert into digested pUC 19 plasmid. Failed. Probably too much X-gal on plate.
August 15
- [http://129.219.2.10/home2/dnalims/fragment/32/21/pfasta/topo0_T7Term.seq Topo 0], [http://129.219.2.10/home2/dnalims/fragment/32/21/pfasta/D168Atopo1_T7Term.seq D168A Topo1], and [http://129.219.2.10/home2/dnalims/fragment/32/21/pfasta/D168Atopo2_T7Term.seq D168A Topo2] sequence results
August 16
- Replated magainin insert + plasmid into the grid. Failed. All blue colonies meaning that no insert.
Tried gel for all gel-isolated fragments. Failed. Did not get a band in the 2000 bp region. Only got things below 200 bp.
October 1
- Minipreps of:
- J61011 + S + L + ALPHA 2B
- J61100 + S + L + ALPHA 2B
- J61100 + S + L + ALPHA 2C
- PLUX2 + RBS + ALPHA 1A
- PLUX2 + RBS + ALPHA 1A (2)
- PLUX + S + L + ALPHA 2C
- J61101 + S + L + ALPHA 1A
- J61101 + S + L + ALPHA 1A (2)
- PLUX2 + RBS + S + L + ALPHA 2B
- PLUX2 + RBS + S + L + ALPHA 2B (2)
- J61101 + S + L + ALPHA 2C
- PLUX + S + L + ALPHA 2B
- Ran Twice when finding concentrations:
- J61101 + S + L + ALPHA 1A
- J61101 + S + L + ALPHA 2B
- Restricted all the above and:
- Strep + Linker + OMEGA
- Strep + Linker-4 + OMEGA
- with:
- X+P
- Ligated into pSB1C3 shipping vector and transformed into BL21(DE3) cells.
- Prepared all 14 above samples for sequencing.
