Template:KIT-Kyoto-Augsut11

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== Electrophoretic run (Practice) ==
 
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Time: From 9:00 to 18:00<BR>
 
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[Member] Iwaki, Fukuyama, Takeuchi, Usui, Adachi<BR>
 
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[Details of Experiment]<BR>
 
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(1)We made 1% Agarose Gel by using Agarose 0.2g and TEA 20μL.<BR>
 
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(2)We mixed DNA 5μL, Marker 1μL and Loading Buffer 1μL.<br>
 
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We applied each 5μL of them to gel.We applied Marker 5μL to the far left lane.<BR>
 
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(3) 100V, 30min electrophoresed<BR>
 
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(4)Gel soaked in EtBr for 20min.<BR>
 
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(5) Band Shooting. <BR>
 

Latest revision as of 12:58, 6 September 2010