Team:Chiba/Sender experiments/Senders(JW1908) T9002(JW1908)

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design

Method

  1. Transformed Senders into E.coli strains(JW1908) and Receiver into E.coli strain(JW1908).
  2. Inoculated them independently in liquid media. Incubated at 37°C 12h
  3. Mixed them.
  4. Incubated at 37°C.
  5. Measured intensity of green fluorescence at regular time intervals.

more details...

Reaction temparature:37°C

  • センダーの培養液:500μL、レシーバの培養液:500μL
Fig.  
E.coli strain,BBa_K084007:JW1908,BBa_T9002:JW1908,37°C,Receiver cells/Sender cells = 1.
Fig.  
E.coli strain,BBa_K084007:JW1908,BBa_T9002:JW1908,37°C,Receiver cells/Sender cells = 1.

Reaction temparature:30°C

  • センダーの培養液:500μL、レシーバの培養液:500μL
Fig.  
E.coli strain,Senders:JW1908,BBa_T9002:JW1908,30°C,Receiver cells/Sender cells = 1.
Fig.  
E.coli strain,Senders:JW1908,BBa_T9002:JW1908,30°C,Receiver cells/Sender cells = 1.


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