Glasgow/Wetlab/Week1
From 2007.igem.org
(Difference between revisions)
(→Friday 6th July 2007) |
(→Friday 6th July 2007) |
||
| Line 91: | Line 91: | ||
#Started designing primers for amplification and site directed mutagenesis of DmpR and DmpR #24 (see [[Glasgow/Wetlab/Protocols#Protocol 4: Primer Design|Protocol 4]]). | #Started designing primers for amplification and site directed mutagenesis of DmpR and DmpR #24 (see [[Glasgow/Wetlab/Protocols#Protocol 4: Primer Design|Protocol 4]]). | ||
<br> | <br> | ||
| - | [[Glasgow/ | + | [[Glasgow/Glasgow/Wetlab/Week1|<font face=georgia color=#99CCFF size=4>Next <br> Week</font>]] |
---- | ---- | ||
Revision as of 12:53, 28 September 2007
| https://static.igem.org/mediawiki/2007/thumb/c/cc/Uog.jpg/50px-Uog.jpg | Back To Glasgow's Main Page | Back To Glasgow's Wetlab Log |
|---|
| Protocols | References | Resources | Orders | Biobricks Used | Gels |
Contents |
Week 1
Tuesday 3rd July 2007
- Maija and Christine prepared LB broth and LB agar with Protocol 1. Made 4 batches of plates, 2 with kanamycin and 2 with carbenicillin.
Wednesday 4th July 2007
- All wetlab researched BioBricks.
- Reporter constructs and mini-Tn5 stocks looked out.
- Streaked the following:
- P. putida PAW 340 pJAK14 (Carb. plate)
- Tn5 lux AB (Carb. plate)
- Mini-Tn5 lux AB (Carb. plate)
- P. fluorescens NCIMB 9815 (Carb. plate)
- P. putida KT2440 (LB)
- JM109 pBluescript 5k+ (Carb. plate)
- Mini-Tn5 Tc (Carb. Plate)
- pQF52 (Carb. plate)
- P. fluorescens 9815 (LB)
- E. coli pJAK14 (Km plate)
- Il DntR in pOF52 (Carb. plate)
- pUCINR in Ω strain C (Carb. plate)
- pGLTUR (Carb. plate)
- Mini-Tn5 Kan (Carb. plate)
- Mini-Tn5 Sm/Sp (Carb. plate)
- Mini-Tn5 1cc2 (Carb. plate)
- E. coli Sa1 (LB)
- DmpR #24 (Carb. plate)
- Mini-Tn5 lac 32 in E. coli 517 (Carb. plate)
- Mini-Tn5 Tc (Carb. Plate)
- Mini-Tn5 Cm (Carb. plate)
- DmpR WT (Carb. plate)
- E.coli sm 10 pESD15 Tn5 GFP (Carb. plate)
- pUJ8 (Carb. Plate)
Thursday 5th July 2007
- BioBricks – Maija and Scott transformed using Protocol 2.
BioBrick Part Function Chassis Plasmid Kit Plate Location (Plate/Well) [http://partsregistry.org/Part:BBa_P1010 Bba_p1010] Construction plasmid E. coli DB3.1 pSB1A10 4/7A " " " pSB1A10 4/11E " " " pSB3K3 4/11C [http://partsregistry.org/Part:BBa_I52001 Bba_I52001] High copy-number construction plasmid E. coli TOP10
should have been DB3.1pSB4A5 4/5I " " " pSB4K5 4/5D " " " pSB4K5 4/6D " " " pSB3K5 4/6B " " " pSB4A5 4/6E [http://partsregistry.org/Part:BBa_J23119 Bba_J23119] Strong constitutive promoter E. coli TOP10 pSB1A2 3/19A [http://partsregistry.org/Part:BBa_R0062 Bba_R0062] HSL & LuxR-inducible promoter E. coli TOP10 pSB1A2 1/9G [http://partsregistry.org/Part:BBa_J04500 Bba_J04500] IPTG-inducible promoter + RBS E. coli TOP10 pSB1AK3 1/16P [http://partsregistry.org/Part:BBa_E0040 Bba_E0040] Promoter-less GFP E. coli TOP10 pSB1A2 1/5H - Maia and Christine researched restriction enzymes for the reporter constructs and Mini-Tn5s streaked on 4/7/07 and digested some. Had planned to make biobricks using Mini-Tn5s etc but discovered that [http://partsregistry.org/Part:BBa_J61206 a previous attempt to use transposable elements to make biobricks] had been unsuccessful due to scarring at the restriction site.
Friday 6th July 2007
- Maija and Christine made 10x stocks for M9 (see Protocol 3.2 - M9).
- Tutorial in [http://www.mbio.ncsu.edu/BioEdit/bioedit.html BioEdit] and [http://biotools.umassmed.edu/bioapps/primer3_www.cgi Primer3].
- Started designing primers for amplification and site directed mutagenesis of DmpR and DmpR #24 (see Protocol 4).
| https://static.igem.org/mediawiki/2007/thumb/c/cc/Uog.jpg/50px-Uog.jpg | Back To Glasgow's Main Page | Back To Glasgow's Wetlab Log |
|---|
