Team:KIT-Kyoto/Protocol

From 2010.igem.org

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<table width="700px">
<table width="700px">
<tr><td width="50%">'''Japanese'''</td><td>'''English'''</td></tr>
<tr><td width="50%">'''Japanese'''</td><td>'''English'''</td></tr>
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<tr><td><a href="#TF>[[#tf|トランスフォーメーション]]</td><td>[[#tfeng|Bacterial transformation]]</td></tr>
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<tr><td>[[#tf|トランスフォーメーション]]</td><td>[[#tfeng|Bacterial transformation]]</td></tr>
<tr><td>[[#al|アルカリミニプレップ]]</td><td>[[#aleng|DNA miniprep]]</td></tr>
<tr><td>[[#al|アルカリミニプレップ]]</td><td>[[#aleng|DNA miniprep]]</td></tr>
<tr><td>[[#pcr|ポリメラーゼ連鎖反応(PCR)]]</td><td>[[#pcreng|Polymerase Chain Reaction(PCR)]]</td></tr>
<tr><td>[[#pcr|ポリメラーゼ連鎖反応(PCR)]]</td><td>[[#pcreng|Polymerase Chain Reaction(PCR)]]</td></tr>
<tr><td>[[#re|制限酵素処理]]</td><td>[[#reeng|DNA digestion by restriction enzymes]]</td></tr>
<tr><td>[[#re|制限酵素処理]]</td><td>[[#reeng|DNA digestion by restriction enzymes]]</td></tr>
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<tr><td>[[#agar|アガロースゲル電気泳動]]</td><td>[[#agareng|Agarose gel electrophoresis]]</a></td></tr>
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<tr><td>[[#agar|アガロースゲル電気泳動]]</td><td>[[#agareng|Agarose gel electrophoresis]]</td></tr>
<tr><td>[[#gel|ゲルからのDNA抽出]]</td><td>[[#geleng|Isolation of DNA fragments from agarose gel]]</td></tr>
<tr><td>[[#gel|ゲルからのDNA抽出]]</td><td>[[#geleng|Isolation of DNA fragments from agarose gel]]</td></tr>
<tr><td>[[#lig|ライゲーション]]</td><td>[[ligeng|DNA ligation]]</a></td></tr>
<tr><td>[[#lig|ライゲーション]]</td><td>[[ligeng|DNA ligation]]</a></td></tr>
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<tr><td>[[#seq|シークエンス]]</td><td>[[#seqeng|Sequencing]]</td></tr>
<tr><td>[[#seq|シークエンス]]</td><td>[[#seqeng|Sequencing]]</td></tr>
<tr><td>[[#gly|グリセロールストック]]</td><td>[[#glyeng|Glycerol stock]]</td></tr>
<tr><td>[[#gly|グリセロールストック]]</td><td>[[#glyeng|Glycerol stock]]</td></tr>
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<tr><td>[[#lb|LB培地]]</a></td><td>[[#lbeng|LB culture medium]]</td></tr>
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<tr><td>[[#lb|LB培地]]</td><td>[[#lbeng|LB culture medium]]</td></tr>
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<tr><td>[[#yt|2×YT培地]]</a></td><td>[[#yteng|2×YT culture medium]]</td></tr>
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<tr><td>[[#yt|2×YT培地]]</td><td>[[#yteng|2×YT culture medium]]</td></tr>
<tr><td>[[#sob|SOB培地]]</td><td>[[#sobeng|SOB culture medium]]</td></tr>
<tr><td>[[#sob|SOB培地]]</td><td>[[#sobeng|SOB culture medium]]</td></tr>
<tr><td>[[#soc|SOC培地]]</td><td>[[#soceng|SOC culture medium]]</td></tr>
<tr><td>[[#soc|SOC培地]]</td><td>[[#soceng|SOC culture medium]]</td></tr>

Revision as of 08:39, 23 October 2010



Home > Notebook > Protocol
Language : English / Japanese

About protocol

PROT.PNG
As it is of common knowledge, iGEM is carried out within the framework of a protocol common to all teams. Whereas most of the teams are registered on this page, we have uploaded not only the English protocol but also the Japanese one, e.g., our mother tongue version. This is the common protocol with some improvements after we translated it into Japanese.Publishing the Japanese protocol in will be of help to other new Japanese teams in the future. Furthermore, this will be linked to an improvement of iGEM’s name identification in Japan and will enhance the public recognition of synthetic biology. It will also promote Science and Communication among people within not only the scientific but with the non-scientific communities as well. We believe that these improvements will constitute a contribution to the illustration of the public in general.


Contents

JapaneseEnglish
トランスフォーメーションBacterial transformation
アルカリミニプレップDNA miniprep
ポリメラーゼ連鎖反応(PCR)Polymerase Chain Reaction(PCR)
制限酵素処理DNA digestion by restriction enzymes
アガロースゲル電気泳動Agarose gel electrophoresis
ゲルからのDNA抽出Isolation of DNA fragments from agarose gel
ライゲーションDNA ligation</a>
コンピテント細胞の作製Preparing chemically competent cells
シークエンスSequencing
グリセロールストックGlycerol stock
LB培地LB culture medium
2×YT培地2×YT culture medium
SOB培地SOB culture medium
SOC培地SOC culture medium

Protocol

トランスフォーメーションBacterial transformation
↓氷上でコンピテント細胞(DH5α:大腸菌株)を融かす↓Thaw competent cells(DH5 Alpha:E.coli strain) on ice.
↓前もって冷やしておいた1.5 mlチューブに100 μlのコンピテント細胞を分注する、余ったコンピテント細胞は-80 ℃の冷凍庫に戻す↓Aliquot 100 μl cells into pre-chilled 1.5 ml tube.Put excess competent cells back into the -80℃ freezer.
↓DNAをチューブに1~5 μl加えて、氷上で30分間冷やす↓Add DNA (1 to 5 μl) to tube, incubate on ice for 30 minutes.
↓42 ℃で45秒間熱ショックを与える↓Heat shock the cells at 42 ℃ for 45 seconds.
↓0.9 mlのSOC培地を加える↓Add 0.9 ml SOC medium.
↓37 ℃で1時間、振りながら回復培養する↓Rescue at 37 ℃ for 1 hour, shaking.
↓1 mlをLBプレート(+amp,+kan,+camのいずれか)にまく↓Spread 1 ml on LB plates(Either +amp,+kan or +cam)
↓37 ℃で一晩培養する↓Clutivate overnight in 37 ℃ .