Template:Kyoto/Notebook/Aug 28

From 2013.igem.org

(Difference between revisions)
(Ligation)
(Gel Extraction: (editor:kojima))
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===Gel Extraction===
===Gel Extraction===
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<!-- こっから -->
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<div class="experiment">
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<span class="author">No name</span>
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{| class="wikitable"
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!Lane||DNA
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|-
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|1||100bpladder||--
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|-
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|3||SasA(8/27 Genome PCR production)
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|-
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|5||RpaA(8/27 Genome PCR production)
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|-
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|7||RpaB(8/27 Genome PCR production)
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|-
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|9||PkaiBC(8/27 Genome PCR production)
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|}
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[[File:igku_xxbeforexx.xxx]]<br>
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[[File:igku_xxafterxx.xxx]]<br>
 +
===Colony PCR===
===Colony PCR===
===Restriction Enzyme Digestion===
===Restriction Enzyme Digestion===

Revision as of 06:08, 21 September 2013

Contents

Aug 28

Electrophoresis

No name

LaneSample
1100bp
2SasA
3RpaA
4RpaB
5PkaiBC
6PCR NC
7100bp

File:Igku xxxxxx.xxx

Miniprep

No name

DNAconcentration[µg/mL]260/280260/230
8/27 Plux173.81.951.45

Ligation

No name

stateVectorInserter
experiment8/71 DT-13.08.0
  • Samples were evaporeted used evaporator into about 3 µL.
sampleMilliQLigation Hightotal
343.510.5
  • incubate one hour at 16 °C

Gel Extraction

No name

LaneDNA
1100bpladder--
3SasA(8/27 Genome PCR production)
5RpaA(8/27 Genome PCR production)
7RpaB(8/27 Genome PCR production)
9PkaiBC(8/27 Genome PCR production)

File:Igku xxbeforexx.xxx
File:Igku xxafterxx.xxx

Colony PCR

Restriction Enzyme Digestion

Electrophoresis

Gel Extraction

Colony PCR

Liquid Culture

Ligation

===Liquid Culture===