Team:Warsaw/Calendar-Stage1/9 July 2010

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<div class="note"> What you were doing [people who were working]</div>
 
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<br>1. something about your task,
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<br> 9.07.2010 Friday
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<a href="http://partsregistry.org/Part:BBa_J61100">this is how to link a part from registry,</a>
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<br>
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[and here go some comments, reaction mixtures etc.]
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<br><div class="note"> Cloning GFP-terminator behind RBSes - approach 2 [Ania P., ..]</div>
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<br>2. Something more about your task
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<br>1. Electrophoresis of samples from 08.07 (samples 39- to the end) 
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<br>2. Choice of proper clones based on these two electrophoresis results (08-09.07):
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<br>  B0030/GFP -> sample 7.2G,
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<br>  B0031/GFP -> sample 8.1E,
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<br>  B0032/GFP -> sample 9.1A,
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<br>  B0033/GFP -> sample 10.1F,
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<br>  B0034/GFP -> sample 11.1P.
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<br>3. DNA of these clones used to transformation.
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<br><div class="note">Preparing glycerol stocks of Anderson's RBSes/GFP-terminator [Ania P., ..]</div>
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<br> 1. Set up 2 ml liquid culture of clones obtained on the plates with ampicillin (from 7.07).
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Revision as of 16:08, 31 July 2010

Example Tabs


9.07.2010 Friday

Cloning GFP-terminator behind RBSes - approach 2 [Ania P., ..]

1. Electrophoresis of samples from 08.07 (samples 39- to the end)
2. Choice of proper clones based on these two electrophoresis results (08-09.07):
B0030/GFP -> sample 7.2G,
B0031/GFP -> sample 8.1E,
B0032/GFP -> sample 9.1A,
B0033/GFP -> sample 10.1F,
B0034/GFP -> sample 11.1P.
3. DNA of these clones used to transformation.
Preparing glycerol stocks of Anderson's RBSes/GFP-terminator [Ania P., ..]

1. Set up 2 ml liquid culture of clones obtained on the plates with ampicillin (from 7.07).

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