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Team:Evry/Notebook
From 2014.igem.org
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<!--*************************************** WEEK XX ****************************************************************--> | <!--*************************************** WEEK XX ****************************************************************--> | ||
| - | <h1 id="week1">Week 1: 4<sup>th</sup>August - | + | <h1 id="week2">Week 2: 28<sup>th</sup> July - 3<sup>th</sup> August</h1> |
| + | <h2>friday, 1th August</h2> | ||
| + | |||
| + | <b><div align="center">Protocol for transformation </b><br/></div> | ||
| + | |||
| + | We transformed TOP 10 E. coli with plasmid of conjugation. This plasmid contains erythromycin like resistance cassette. I plated them on LB-Agar with erythomycin antibiotic. | ||
| + | |||
| + | |||
| + | <h2>sunday, 3st August</h2> | ||
| + | |||
| + | <b><div align="center">Transformed cells </b><br/></div> | ||
| + | The cells transformed groth in the plate with erythromycin. I take one colonie in 3mL LB with erythromycin. | ||
| + | |||
| + | <b><div align="center">Tests culture pseudovibrio with medium </b><br/></div> | ||
| + | I take 1mL culture in M9 (aa and 3% NaCL)to 3 differents medium :<br/> | ||
| + | 9mL MB<br/> | ||
| + | 9mL M9<br/> | ||
| + | 9mL 2xYT<br/> | ||
| + | 9mL LB<br/> | ||
| + | |||
| + | |||
| + | |||
| + | <!--*************************************** WEEK XX ****************************************************************--> | ||
| + | <h1 id="week1">Week 1: 4<sup>th</sup>August - 10<sup>rd</sup> August</h1> | ||
<h2>Monday, 4th August</h2> | <h2>Monday, 4th August</h2> | ||
| + | <b><div align="center">Tests culture pseudovibrio with medium </b><br/></div> | ||
| + | MB : the cells growth<br/> | ||
| + | M9 : the cells growth<br/> | ||
| + | 2xYT : the cells growth<br/> | ||
| + | LB : the cells don't growth<br/> | ||
| + | |||
| + | |||
| + | <b><div align="center">Plasmid DNA puriication </b><br/></div> | ||
A culture of E.coli transformed with plasmide of conjugation. A plasmid purification is realised with kit NucleoSpin. | A culture of E.coli transformed with plasmide of conjugation. A plasmid purification is realised with kit NucleoSpin. | ||
After that 94,5ng.L-1 is purified. | After that 94,5ng.L-1 is purified. | ||
Revision as of 18:50, 5 August 2014
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9mL MB
9mL M9
9mL 2xYT
9mL LB
M9 : the cells growth
2xYT : the cells growth
LB : the cells don't growth
Week 2: 28th July - 3th August
friday, 1th August
Protocol for transformation
We transformed TOP 10 E. coli with plasmid of conjugation. This plasmid contains erythromycin like resistance cassette. I plated them on LB-Agar with erythomycin antibiotic.
sunday, 3st August
Transformed cells
The cells transformed groth in the plate with erythromycin. I take one colonie in 3mL LB with erythromycin.
Tests culture pseudovibrio with medium
I take 1mL culture in M9 (aa and 3% NaCL)to 3 differents medium :9mL MB
9mL M9
9mL 2xYT
9mL LB
Week 1: 4thAugust - 10rd August
Monday, 4th August
Tests culture pseudovibrio with medium
MB : the cells growthM9 : the cells growth
2xYT : the cells growth
LB : the cells don't growth
Plasmid DNA puriication
A culture of E.coli transformed with plasmide of conjugation. A plasmid purification is realised with kit NucleoSpin.
After that 94,5ng.L-1 is purified.
