Team:UT-Tokyo/Notebook
From 2010.igem.org
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Our experiment notebooks (Japanese) can be read [http://www.igem-ut.net/blog/ here (www.igem-ut.net/blog) ]. | Our experiment notebooks (Japanese) can be read [http://www.igem-ut.net/blog/ here (www.igem-ut.net/blog) ]. | ||
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+ | == '''Protocol''' == | ||
+ | |||
+ | === Transformation === | ||
+ | |||
+ | -preparation | ||
+ | ・iGEM parts / ligation products | ||
+ | ・LBbroth (No antibiotic) 500uL | ||
+ | ・TE 15uL | ||
+ | ・competent cells | ||
+ | ・plates | ||
+ | ・ice box | ||
+ | ・heat block(42℃) | ||
+ | |||
+ | -Notice | ||
+ | competent cells | ||
+ | → always onice!!! Melt on ice! Mix DNA as soon as cells melt! | ||
+ | |||
+ | -Protocol | ||
+ | iGEMパーツを解凍する場合 | ||
+ | ↓P200のピペットマンにチップを付け、チップでフィルムに孔を空ける。 | ||
+ | ↓add 15µl TE(MilliQで可)、ピペッティング | ||
+ | ↓1µlをコンピテントセルにいれ30min on ice(コンピに対し1/5倍量以下になるように) | ||
+ | |||
+ | iGEM parts | ||
+ | |||
+ | Hole film with a tip | ||
+ | |||
+ | ↓Add 15 uL TE or MilliQ, pipetting | ||
+ | |||
+ | ↓Mix 1uL with competent cells 50uL | ||
+ | |||
+ | ↓on ice 30 min | ||
+ | |||
+ | ↓42℃ 45 sec | ||
+ | |||
+ | ↓on ice 10 min | ||
+ | |||
+ | ↓Mix LBbroth 300 uL | ||
+ | |||
+ | ↓37℃ 30 min or room temprature 15 min (amp:omittable) | ||
+ | |||
+ | ↓Plate, 37℃ incubation over night | ||
+ | |||
+ | |||
+ | |||
+ | |||
+ | Ligation products | ||
+ | |||
+ | ↓Mix ligation products 10uL, competent cells 50uL | ||
+ | |||
+ | ↓on ice 30 min | ||
+ | |||
+ | ↓42℃ 45 sec | ||
+ | |||
+ | ↓on ice 10 min | ||
+ | |||
+ | ↓Mix LBbroth 300 uL | ||
+ | |||
+ | ↓37℃ 30 min or room temprature 15 min (amp:omittable) | ||
+ | |||
+ | ↓Plate, 37℃ incubation over night | ||
+ | |||
+ | |||
</div> | </div> | ||
{{UT-Tokyo_FOOTER}} | {{UT-Tokyo_FOOTER}} |
Revision as of 06:59, 19 August 2010
Notebook
Our experiment notebooks (Japanese) can be read [http://www.igem-ut.net/blog/ here (www.igem-ut.net/blog) ].
Protocol
Transformation
-preparation ・iGEM parts / ligation products ・LBbroth (No antibiotic) 500uL ・TE 15uL ・competent cells ・plates ・ice box ・heat block(42℃)
-Notice competent cells → always onice!!! Melt on ice! Mix DNA as soon as cells melt!
-Protocol iGEMパーツを解凍する場合 ↓P200のピペットマンにチップを付け、チップでフィルムに孔を空ける。 ↓add 15µl TE(MilliQで可)、ピペッティング ↓1µlをコンピテントセルにいれ30min on ice(コンピに対し1/5倍量以下になるように)
iGEM parts
Hole film with a tip
↓Add 15 uL TE or MilliQ, pipetting
↓Mix 1uL with competent cells 50uL
↓on ice 30 min
↓42℃ 45 sec
↓on ice 10 min
↓Mix LBbroth 300 uL
↓37℃ 30 min or room temprature 15 min (amp:omittable)
↓Plate, 37℃ incubation over night
Ligation products
↓Mix ligation products 10uL, competent cells 50uL
↓on ice 30 min
↓42℃ 45 sec
↓on ice 10 min
↓Mix LBbroth 300 uL
↓37℃ 30 min or room temprature 15 min (amp:omittable)
↓Plate, 37℃ incubation over night