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Team:Tokyo Metropolitan/Notebook/Pattern/2010/08/06
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| - | == | + | ==1：Making LB plate (20ml×20)== |
＜Member＞<br /> | ＜Member＞<br /> | ||
Mariko, tomy, easily, naoto, nito, Taka, watachin | Mariko, tomy, easily, naoto, nito, Taka, watachin | ||
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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. | ||
| - | == | + | ==2：Scattering E-coli (having BioBrick plasmid) on LB plate== |
＜Member＞<br /> | ＜Member＞<br /> | ||
tomy, easily, naoto, nito | tomy, easily, naoto, nito | ||
Revision as of 12:43, 3 September 2010
2010/08/06
1：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.
2：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℃.
