Team:Tokyo Metropolitan/Notebook/Pattern/2010/08/06

From 2010.igem.org

(Difference between revisions)
(2010/08/06)
(Experiment1:Making LB plate (20ml×20))
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1 Prepared 400ml solution to contain Yeast extract 2.0g, Peptone 2.0g, Glucose 40.0g, NaCl 2.0g and Agerose 6.0g.
1 Prepared 400ml solution to contain Yeast extract 2.0g, Peptone 2.0g, Glucose 40.0g, NaCl 2.0g and Agerose 6.0g.
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4 Cooled and dried divided solutions in Petri dishes. After Cooling and drying well, kept these in refrigerator.
4 Cooled and dried divided solutions in Petri dishes. After Cooling and drying well, kept these in refrigerator.
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==Experiment2;Scattering E-coli (having BioBrick plasmid) on LB plate==
==Experiment2;Scattering E-coli (having BioBrick plasmid) on LB plate==

Revision as of 12:52, 15 August 2010


2010/08/06

Experiment1:Making LB plate (20ml×20)

<Member>Mariko, tomy, easily, naoto, nito, Taka, watachin

<Materials>
・Yeast extract 2.0g

・Peptone 2.0g

・Glucose 40.0g

・NaCl 2.0g

・Agerose 6.0g

・Ampcillim 0.4mg

・Dropped water 400ml


<Protocol>
1 Prepared 400ml solution to contain Yeast extract 2.0g, Peptone 2.0g, Glucose 40.0g, NaCl 2.0g and Agerose 6.0g.

2 Divided up 400ml solution into two Erlenmeyer flasks, and sealed with aluminum. Afterwards , started autoclave(121℃,20min)

3 After finished autoclave, in cleanbench, added 0.2ml Ampcillm to each of the solutions. Afterwards, divided solutions into twenty Petri dishes.

4 Cooled and dried divided solutions in Petri dishes. After Cooling and drying well, kept these in refrigerator.

Experiment2;Scattering E-coli (having BioBrick plasmid) on LB plate

<Member>tomy, easily, naoto, nito

<Materials>

・LB plate×4

・E-coli (having BBa_I1732901 plasmid)

・E-coli (having BBa_K208017 plasmid)


<Protocol>

1 Sterilized Inoculation loop by flame. After Sterilization, pick up E-coli by Inoculation loop、and then scatter on LB plate.

2 Incubated these plate at 37℃.