Team:Freiburg/Notebook/15 June

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=='''??.Labday'''==
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<a href="https://2011.igem.org/Team:Freiburg/Notebook/14_June">Previous entry</a>
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<a href="https://2011.igem.org/Team:Freiburg/Notebook"> 15 June </a>
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<a href="https://2011.igem.org/Team:Freiburg/Notebook/16_June">Next entry</a>
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==PCR for Ccas and CcaR==
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==<span style="color:green;">green light receptor</span>==
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===PCR for Ccas and CcaR===
'''Investigators: Julia'''
'''Investigators: Julia'''
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0,5 µl Phusion<br/>
0,5 µl Phusion<br/>
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===Gel with PCR products: Ccas, Ccar===
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the first gel was stained with G-Stain, but adding G-Stain to the GeneRuler destroyed it.
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Second Gel was post-stained with ethidium-bromid, the bands for  CcaS &CcaR were at some place, nothing really clear.
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<span style= "color:blue;"> Comments: Has to be repeated. Either repeat the PCR or run a new gel with higher agarose concentration.</span>
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==Miniprep==
==Miniprep==
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Miniprep PR4a, PR4b, PR8a, PR8b, PR9a, PR9b<br/>
Miniprep PR4a, PR4b, PR8a, PR8b, PR9a, PR9b<br/>
measurement of nanodrop was ok<br/>
measurement of nanodrop was ok<br/>
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==3A-assembly:Digestion==
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'''Investigators: Theo, Jakob'''
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Restriction digest of plasmid constructs (3A Assemblies PR1, PR2, PR3, PR4, PR5, PR7, PR8, Pr9)<br/>
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Protocol: Mix => for one reaction, total volume 10µl<br/>
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3µl DNA<br/>
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1µl NEBuffer4<br/>
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1µl BSA<br/>
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0,5µl Enzym<br/>
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==<span style="color:orange;">Lysis cassette</span>==
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===Transformation===
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'''Investigators: Sandra'''
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Transformation of BBa_K124014 bacteriophage Holin Gene pS105<br/>
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plated out at 3:36pm in plates with ampicillin
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'''Investigators: Julia'''
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Transformation of BBa_E0040 green fluorescent protein. Ampicillin resistance.
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Latest revision as of 01:20, 22 September 2011


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