Team:Paris/July 30
From 2008.igem.org
(→Results of transformations) |
(→Results of transformations) |
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{{Paris/Calendar_Links|July 29|July 31}} | {{Paris/Calendar_Links|July 29|July 31}} | ||
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|align="center"|L103 | |align="center"|L103 | ||
- | |align="center"|Strong rbs - | + | |align="center"|Strong rbs - mRFP<br>D129 (BV) - D122 (BI) |
|align="center"|Amp | |align="center"|Amp | ||
|align="center"|a lot | |align="center"|a lot | ||
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|align="center"|L107 | |align="center"|L107 | ||
- | |align="center"|Strongest promoter - ECFP<br>D103 (BV) - | + | |align="center"|Strongest promoter - ECFP<br>D103 (BV) - D130 (BI) |
|align="center"|Amp | |align="center"|Amp | ||
|align="center"|a lot | |align="center"|a lot | ||
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|align="center"|L108 n°2 <br>(the right one) | |align="center"|L108 n°2 <br>(the right one) | ||
- | |align="center"|Strong promoter - gfp Tripart<br>D103 (BV) - | + | |align="center"|Strong promoter - gfp Tripart<br>D103 (BV) - D131 (BI) |
|align="center"|Amp | |align="center"|Amp | ||
|align="center"|+/- 100 | |align="center"|+/- 100 | ||
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|align="center"|L112 | |align="center"|L112 | ||
- | |align="center"|Weak promoter - gfp<br>D104 (BV) - D131 (BI) | + | |align="center"|Weak promoter - gfp tripart<br>D104 (BV) - D131 (BI) |
|align="center"|Amp | |align="center"|Amp | ||
|align="center"|a lot | |align="center"|a lot | ||
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|align="center"|L120 | |align="center"|L120 | ||
- | |align="center"|tetR repressible - ECFP<br>D106 (BV) - D130 (BI) | + | |align="center"|tetR repressible promoter - ECFP<br>D106 (BV) - D130 (BI) |
|align="center"|Amp | |align="center"|Amp | ||
|align="center"|a lot | |align="center"|a lot | ||
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|align="center"|L121 | |align="center"|L121 | ||
- | |align="center"| | + | |align="center"|tetR repressible promoter - gfp tripart<br>D106 (BV) - D131 (BI) |
|align="center"|Amp | |align="center"|Amp | ||
|align="center"|a lot | |align="center"|a lot | ||
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|align="center"|L123 | |align="center"|L123 | ||
- | |align="center"|RBS lasI - | + | |align="center"|RBS lasI - gfp tripart<br>D107 (BV) - D131 (BI) |
|align="center"|Amp | |align="center"|Amp | ||
|align="center"|1 | |align="center"|1 | ||
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|align="center"|L124 | |align="center"|L124 | ||
- | |align="center"|Strongest RBS - | + | |align="center"|Strongest RBS - mRFP<br>D102 (BV) - D122 (BI) |
|align="center"|Amp | |align="center"|Amp | ||
|align="center"|a lot | |align="center"|a lot | ||
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|align="center"|L126 | |align="center"|L126 | ||
- | |align="center"|Strongest RBS (1)- LacR activator (+LVA)<br>D102 (BV) - | + | |align="center"|Strongest RBS (1)- LacR activator (+LVA)<br>D102 (BV) - D114 (BI) |
|align="center"|Amp | |align="center"|Amp | ||
|align="center"|no dish found!!! | |align="center"|no dish found!!! | ||
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|align="center"|Amp | |align="center"|Amp | ||
|align="center"|0 | |align="center"|0 | ||
- | |align="center"| | + | |align="center"|ok |
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|align="center"|C2 | |align="center"|C2 | ||
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|align="center"|Amp | |align="center"|Amp | ||
|align="center"|5 | |align="center"|5 | ||
- | |align="center"| | + | |align="center"|ok |
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|align="center"|C3 | |align="center"|C3 | ||
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|align="center"|Amp | |align="center"|Amp | ||
|align="center"|+/- 100 | |align="center"|+/- 100 | ||
- | |align="center"| | + | |align="center"|ok |
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|align="center"|C4 | |align="center"|C4 | ||
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|align="center"|Amp | |align="center"|Amp | ||
|align="center"|+/- 20 | |align="center"|+/- 20 | ||
- | |align="center"| | + | |align="center"|ok |
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|align="center"|C5 | |align="center"|C5 | ||
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|align="center"|Amp | |align="center"|Amp | ||
|align="center"|+/- 100 | |align="center"|+/- 100 | ||
- | |align="center"| | + | |align="center"|ok |
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|align="center"|C6 | |align="center"|C6 | ||
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|align="center"|Amp | |align="center"|Amp | ||
|align="center"|+/- 100 | |align="center"|+/- 100 | ||
- | |align="center"| | + | |align="center"|ok |
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|align="center"|C7 | |align="center"|C7 | ||
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|align="center"|Kana | |align="center"|Kana | ||
|align="center"|0 | |align="center"|0 | ||
- | |align="center"| | + | |align="center"|ok |
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|align="center"|C8 | |align="center"|C8 | ||
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|align="center"|Amp | |align="center"|Amp | ||
|align="center"|+/- 20 | |align="center"|+/- 20 | ||
- | |align="center"| | + | |align="center"|ok |
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|align="center"|C9 | |align="center"|C9 | ||
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|align="center"|Amp | |align="center"|Amp | ||
|align="center"|0 | |align="center"|0 | ||
- | |align="center"| | + | |align="center"|ok |
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|align="center"|C10 | |align="center"|C10 | ||
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|align="center"|Amp | |align="center"|Amp | ||
|align="center"|0 | |align="center"|0 | ||
- | |align="center"| | + | |align="center"|ok |
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|align="center"|C11 | |align="center"|C11 | ||
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|align="center"|Amp | |align="center"|Amp | ||
|align="center"|0 | |align="center"|0 | ||
- | |align="center"| | + | |align="center"|ok |
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|align="center"|C12 | |align="center"|C12 | ||
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|align="center"|Amp | |align="center"|Amp | ||
|align="center"|+/- 10 | |align="center"|+/- 10 | ||
- | |align="center"| | + | |align="center"|ok |
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|align="center"|Positive control | |align="center"|Positive control | ||
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|align="center"|Amp | |align="center"|Amp | ||
|align="center"|155 (transformation <br> efficiency:1.5*10^7/ug) | |align="center"|155 (transformation <br> efficiency:1.5*10^7/ug) | ||
- | |align="center"| | + | |align="center"|ok |
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==> '''Conclusion :'''Each of the samples was succesfully digested and purified except for the sample D108. It seems that the QIAprep columms (from the QIAGEN Minipreps kit) can be used instead of the QIAquick columms (for DNA Gel Extraction). | ==> '''Conclusion :'''Each of the samples was succesfully digested and purified except for the sample D108. It seems that the QIAprep columms (from the QIAGEN Minipreps kit) can be used instead of the QIAquick columms (for DNA Gel Extraction). | ||
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== '''PCR Screening of Ligation Transformants'''== | == '''PCR Screening of Ligation Transformants'''== | ||
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* 10µl of screening PCR (gel n°3(1), 13, 14) | * 10µl of screening PCR (gel n°3(1), 13, 14) | ||
* migration ~30min at 100W on '''0,8%''' gel | * migration ~30min at 100W on '''0,8%''' gel | ||
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===Results=== | ===Results=== |
Latest revision as of 17:03, 13 August 2008
Results of transformations
Analysis of yesterday DNA digestionThe digested DNA of yesterday was analysed one more time by electrophoresis on a 0.8% agarose gel (about 30 minutes at 100 W).
==> Conclusion :Each of the samples was succesfully digested and purified except for the sample D108. It seems that the QIAprep columms (from the QIAGEN Minipreps kit) can be used instead of the QIAquick columms (for DNA Gel Extraction).
PCR Screening of Ligation TransformantsUse of 8 clones of Ligation transformants for screening PCR
Protocol of screening PCR
Conditions of electrophoresis
Results
But we don't observe results for L102(3), L102(6), L103(4), L106(1), L106(2), L106(4), L111(1) Migration of an another gel for this sample...
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