Team:Grenoble/Biology/Notebook/August/week 35
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We did some ligations (<a href="https://2012.igem.org/Team:Grenoble/Biology/Protocols/Ligation">protocol</a>) in order to do the | We did some ligations (<a href="https://2012.igem.org/Team:Grenoble/Biology/Protocols/Ligation">protocol</a>) in order to do the | ||
construction: pAra/Bad_RBS_GFP_RBS_Cya and the construcion: pompC_mcherry.<br/> | construction: pAra/Bad_RBS_GFP_RBS_Cya and the construcion: pompC_mcherry.<br/> | ||
+ | </section> | ||
+ | |||
+ | <section> | ||
+ | <h2> Thursday, August 30<span class="exposant">th</span>:</h2> | ||
+ | We did some verification PCRs on miniprep with HF Phusion enzyme (<a href="https://2012.igem.org/Team:Grenoble/Biology/Protocols/PCR_2">protocol</a>) in order to check the | ||
+ | constructions with pompC_mcherry and pAra/Bad_RBS_GFP_RBS_Cya.<br/> | ||
+ | <br/> | ||
Revision as of 03:22, 27 September 2012
August
Week 31 • Week 32 • Week 33 • Week 34 • Week 35Week 35: August 27th to September 02nd
Goal of the week:
We wanted to construct (protocol) the double mutant strains we need for our experiments.We also wanted to assemble pAra/Bad_RBS_GFP_RBS_Cya, pompC_mcherry, TapZ and tu put these constructions on pSB1C3.
Tuesday, August 28th:
We did some verification PCRs on miniprep with HF Phusion enzyme (protocol) in order to check the constructions with pompC_mcherry.To separate (protocol) the PCR products, we prepared a 1.8% TAE agarose gel.
Migration conditions = 100V during 30 min.
In order to reveal the DNA fragments, we used EtBr.
The PCR showed no significant results (data not shown).
We did some digestions (protocol) in order to do the construction: pAra/Bad_RBS_GFP_RBS_Cya and the construcion: pompC_mcherry.