Team:Tokyo Metropolitan/Notebook/Fiber/2010/08/27

From 2010.igem.org

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(New page: ==2010/08/26(Bambi75)== ==Make Plates== ===member=== NEX , Bambi75 and watachin ===Materials=== *RO water 200ml *LB Broth 4g *Cam(50μg/L) 10ml ===Procedure=== ① mix materials. ② D...)
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==2010/08/26(Bambi75)==
 
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==Make Plates==
 
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===member===
 
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NEX , Bambi75 and watachin
 
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===Materials===
 
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*RO water 200ml
 
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*LB Broth 4g
 
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*Cam(50μg/L) 10ml
 
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===Procedure===
 
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① mix materials.
 
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② Divide ①equally and make 10 plates.
 
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==Separation of A.xylinum==
 
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===member===
 
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easily and naoto
 
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===Materials===
 
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*the plate(made on August 25th).
 
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===Procedure===
 
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①extract material 2ml.
 
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②centrifuge ① 10000rpm/5min.
 
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==PCR==
 
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===member===
 
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same above
 
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===Materials===
 
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*2×PCR buffer  25×4μl
 
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*2mM dNTP  10×4μl
 
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*10mM primer(sense)bcsA,B,C and D 2.5μl each
 
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*10mM primer(antisense)bcsA,B,C and D 2.5μl each
 
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*template DNA a little
 
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*Q water 9×4μl
 
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*KOD FX 0.5×4μl
 
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===Procedure===
 
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①mix all materials for 4 tubes.
 
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②elongation
 
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*bcsA,bcsB and bcsC
 
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**94℃ 2min
 
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**98℃ 10sec☆
 
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**55℃ 30sec
 
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**68℃ 4min★
 
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**68℃ 7min
 
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**10℃ ∞
 
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*bcsD
 
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**94℃ 2min
 
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**98℃ 10sec☆
 
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**55℃ 30sec
 
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**68℃ 1min★
 
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**68℃ 7min
 
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**10℃ ∞
 
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※30cycle ☆ to ★.
 
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==PCR==
 
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===member===
 
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NEX , Bambi75 and watachin
 
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===Materials===
 
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*sterilized water 71μl
 
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*Ex taq buffer 10μl
 
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*dNTP mix 8μl
 
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*Ex taq 1μl
 
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*primer(bcsC sense/antisense) 5μl each
 
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===Procedure===
 
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①mix materials
 
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②divide ① into 2 tubes.
 
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③elongation
 
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**95℃ 3min
 
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**96℃ 1min☆
 
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**55℃ 7min
 
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**72℃ 1min★
 
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**10℃ ∞
 
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※30 cycle ☆to★.
 

Latest revision as of 06:08, 8 September 2010