Team:Evry/Notebook/CellCharacterization/Transformation/08-23-2014

From 2014.igem.org

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<u> <b> Amplification of plasmids pBBR1MCS and pRhokHI-2 </b> </u> <br>
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<u> <b> <big><FONT COLOR=#003333>Amplification of plasmids pBBR1MCS and pRhokHI-2 in E.Coli Bl21</font></big></b> </u> <br>
Two plasmids pBBR1MCS and pRhokHI-2 were generously sent by Dr Thomas DREPPER (University Duesseldorf, Dept. of Biology, Institute of Molecular Enzyme Technology)
Two plasmids pBBR1MCS and pRhokHI-2 were generously sent by Dr Thomas DREPPER (University Duesseldorf, Dept. of Biology, Institute of Molecular Enzyme Technology)
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Bowth were transfered into Bl21 electro-competent cells by electroporation (two replicate)   <b>(LIEN PROTO)</b>. <br> After a liquid culture of three hours, cells were plated on LB 1X + Cam (1:1000) and let in incubator overnight.
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Bowth were transfered into Bl21 electro-competent cells by electroporation (two replicate)(1µL of plasmid for 40µL of cells, 1800V). <br> After a liquid culture of three hours, cells were plated on LB 1X + Cam (1:1000) and let in incubator overnight.</p>

Latest revision as of 22:21, 17 October 2014

Picture

Amplification of plasmids pBBR1MCS and pRhokHI-2 in E.Coli Bl21
Two plasmids pBBR1MCS and pRhokHI-2 were generously sent by Dr Thomas DREPPER (University Duesseldorf, Dept. of Biology, Institute of Molecular Enzyme Technology)

plasmidS

Bowth were transfered into Bl21 electro-competent cells by electroporation (two replicate)(1µL of plasmid for 40µL of cells, 1800V).
After a liquid culture of three hours, cells were plated on LB 1X + Cam (1:1000) and let in incubator overnight.

Aug 23