Edinburgh/24 July 2008

From 2008.igem.org

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<ul>
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<li><a href="https://2008.igem.org/Team:Edinburgh" title="Home"><span>Home</span></a></li>
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<li><a href="https://2008.igem.org/Team:Edinburgh/Project" title="Project" rel="dropmenu1_a"><span>The Project</span></a></li>
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<li><a href="https://2008.igem.org/Team:Edinburgh/Team" title="Team" ><span>The Team</span></a></li>
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<li><a href="http://partsregistry.org/cgi/partsdb/pgroup.cgi?pgroup=iGEM2008&group=Edinburgh" title="Project" rel="dropmenu1_a"><span>BioBrick Parts</span></a></li>
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<li><a href="https://2008.igem.org/Team:Edinburgh/Modeling" title="Modelling" rel="dropmenu2_a"><span>Modelling</span></a></li>
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<li><a href="https://2008.igem.org/Team:Edinburgh/Notebook" title="Notebook"><span>Notebook</span></a></li>
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<a href="https://2008.igem.org/Team:Edinburgh/Team">Overview</a>
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<a href="https://2008.igem.org/Team:Edinburgh/Team">Step1</a>
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<a href="https://2008.igem.org/Team:Edinburgh/Team">Step2</a>
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|-
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|align="left" width="150pt"|{{#calendar: title=Edinburgh |year=2008 | month=06}}
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|-
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|align="left" width="150pt"|{{#calendar: title=Edinburgh |year=2008 | month=07}}
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|-
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|align="left" width="150pt"|{{#calendar: title=Edinburgh |year=2008 | month=08}}
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|}
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:::: '''[[Edinburgh/23_July_2008|< Previous Entry]]'''
:::: '''[[Edinburgh/23_July_2008|< Previous Entry]]'''
Line 334: Line 8:
* Purified PCR products P28 (rbs+''crtB'') and P29 (rbs+''crtI''). (OG)
* Purified PCR products P28 (rbs+''crtB'') and P29 (rbs+''crtI''). (OG)
* Double digestions using XbaI/PstI (buffer H) to add P12 (rbs+''dxs''), P15 (rbs+''appY''), P28 (rbs+''crtB'') and P29 (rbs+''crtI'') to Edinbrick1. (Yan, OG)
* Double digestions using XbaI/PstI (buffer H) to add P12 (rbs+''dxs''), P15 (rbs+''appY''), P28 (rbs+''crtB'') and P29 (rbs+''crtI'') to Edinbrick1. (Yan, OG)
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* Double digestion using SacI/SpeI (BufferE) to add P31 (pZntA) to Edinbrick1. (Yan, OG)
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* Double digestion using SacI/SpeI (BufferE) to add P31 (''P<sub>zntA</sub>'') to Edinbrick1. (Yan, OG)
* Purified genomic DNA from ''C. fimi'' culture (made from plate 37, incubated in 25ml bottle at 30C for 48 hours with shaking). Used Promega Wizard Genomic DNA Purification Kit, lysozyme and RNAse+EDTA (as replacement for proprietary RNAse Solution, of which none was left). Final solution left overnight in refrigerator at 4°C. (AM)
* Purified genomic DNA from ''C. fimi'' culture (made from plate 37, incubated in 25ml bottle at 30C for 48 hours with shaking). Used Promega Wizard Genomic DNA Purification Kit, lysozyme and RNAse+EDTA (as replacement for proprietary RNAse Solution, of which none was left). Final solution left overnight in refrigerator at 4°C. (AM)
* Plated ''C. fimi'' culture from plate 37...
* Plated ''C. fimi'' culture from plate 37...

Latest revision as of 20:35, 29 October 2008

< Previous Entry

Week 6

Thursday 24 July 08

  • Purified PCR products P28 (rbs+crtB) and P29 (rbs+crtI). (OG)
  • Double digestions using XbaI/PstI (buffer H) to add P12 (rbs+dxs), P15 (rbs+appY), P28 (rbs+crtB) and P29 (rbs+crtI) to Edinbrick1. (Yan, OG)
  • Double digestion using SacI/SpeI (BufferE) to add P31 (PzntA) to Edinbrick1. (Yan, OG)
  • Purified genomic DNA from C. fimi culture (made from plate 37, incubated in 25ml bottle at 30C for 48 hours with shaking). Used Promega Wizard Genomic DNA Purification Kit, lysozyme and RNAse+EDTA (as replacement for proprietary RNAse Solution, of which none was left). Final solution left overnight in refrigerator at 4°C. (AM)
  • Plated C. fimi culture from plate 37...
    • Incubated in 25ml bottle for 48 hours at 30°C with shaking ... to Plate 48.
    • Incubated in 50ml bottle for 24 hours at 30°C with shaking ... to Plate 49.
    • Incubated in 250ml flask for 24 hours at 30°C with shaking ... to Plate 50. (AM)
  • PCR of cenA (P32), cenB (P33), cenC (P34), cex (P35), annealing 1 min 55°C, extension 90 sec 70°C. Run on Gel 24 - unsuccessful. (AM)


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