Team:SouthBend-Mishawaka-HS/Notebook

From 2011.igem.org

(Difference between revisions)
(May18)
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=May=
=May=
==May18==
==May18==
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Poured 12 LB AMP plates:
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Poured 12 LB AMP plates:(2mg of Ampicillin to 250ml of Agar)<br>
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*2mg of Ampicillin to 250ml of Agar<br><br>
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Obtained a vial of 2 microliters of TOP-10 electrocompetant <i>E. coli</i> cells (44-0003/793762)<br>
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Added 50 microliters of pure water from the Gemini machine<br>
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Added 10 ul of water to well 6E of plate 2, which contained part F2620. Put 2 ul of the diluted DNA and placed in 50 ul of transformation solution (50mm CaCl2, pH 6.1).
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Added 10 ul of water to well 6E of plate 2, which contained part F2620. Put 2 ul of the diluted DNA and placed in 50 ul of transformation solution (50mm CaCl2, pH 6.1).<br>
 +
Incubate on ice for 5 minutes<br>
 +
Heat shocked at 40 degrees Celcius for 50 seconds<br>
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Incubated at 4 degrees Celcius for 5 minutes<br>
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Added 1mL of LB (5-17-11 DG)<br>
   
   
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Revision as of 21:39, 19 May 2011

May

May18

Poured 12 LB AMP plates:(2mg of Ampicillin to 250ml of Agar)
Obtained a vial of 2 microliters of TOP-10 electrocompetant E. coli cells (44-0003/793762)
Added 50 microliters of pure water from the Gemini machine
Added 10 ul of water to well 6E of plate 2, which contained part F2620. Put 2 ul of the diluted DNA and placed in 50 ul of transformation solution (50mm CaCl2, pH 6.1).
Incubate on ice for 5 minutes
Heat shocked at 40 degrees Celcius for 50 seconds
Incubated at 4 degrees Celcius for 5 minutes
Added 1mL of LB (5-17-11 DG)

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