Team:Kyoto/Notebook

From 2012.igem.org

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94°C
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94°C 2min, (98°C 10sec, 68°C 4min)x2cycles, 4°C Hold
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{|class="wikitable"
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16°C, 1h incubate
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!competent cell!!DNA
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Cells were stored on ice for 30min. <br>
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After 42°C 60sec heat shock, cells were stored on ice for 2min.<br>
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Then cells were preincubated at 37°C for 1hr, plated to Kanamycin plate.
==August 10==
==August 10==

Revision as of 13:09, 21 August 2012

August 2

Mutation of FT

Inverse PCR
10xBufer2mM dNTPsprimer fwdprimer revtemplatepolymeraseMilliQTotal
551.51.50.5135.550

94°C 2min, (98°C 10sec, 68°C 4min)x2cycles, 4°C Hold

Dpn1 Digestion
PCR productDpn1
502
37℃,1h incubate
Self-ligation
productMilliQLigaseT4 KinaseTotal
275115

16°C, 1h incubate

Transformation
competent cellDNA
202

Cells were stored on ice for 30min.
After 42°C 60sec heat shock, cells were stored on ice for 2min.
Then cells were preincubated at 37°C for 1hr, plated to Kanamycin plate.

August 10

Golden Gate Assembly method This method helps us to constract some genes quickly and we can design the order of constractions. We are trying to construct a gene cycle composed of 6 genes( pSB1A3, lacI, GFP, RFP, GFP, DT). After this experiment is confirmed to work, we will so some experiment to check how the numbers of promorters influences the strength of transcription.


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