Team:Chiba/Receiver experiments
From 2008.igem.org
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!align="center"|[[Team:Chiba/Acknowledgements|Acknowledgements]] | !align="center"|[[Team:Chiba/Acknowledgements|Acknowledgements]] | ||
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==Receiver crosstalk== | ==Receiver crosstalk== | ||
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+ | ===Design=== | ||
+ | [[Image:Table R chiba.gif|frame|left|Table.1 LuxR family gene]] | ||
+ | センダーとレシーバーを元来とは異なる組み合わせにすることによって、thresholdに達する時間を遅くする。(杉山) | ||
===Method=== | ===Method=== | ||
===Result=== | ===Result=== | ||
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+ | ==Change Receiver's Copy Number== | ||
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- | + | ===Design=== | |
+ | |||
+ | レシーバーのコピーナンバーを減らすことで、thresholdに達するまでの時間を伸ばす。 | ||
+ | (小林) | ||
===Method=== | ===Method=== | ||
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- | * | + | *High Copy Receiver[http://partsregistry.org/Part:BBa_T9002 BBa_T9002 (AHL Reporter)] |
- | + | ||
- | [ | + | |
- | + | [[Image:T9002.copy-number-change Chiba.gif]] | |
- | [[Image: | + | |
- | + | *Medium Copy Receiver | |
- | # Transformed sender (Ptet- | + | [[Image:Low-copy-Receiver Chiba.gif]] |
- | # Inoculated | + | |
- | # Inoculated again in liquid media upto about OD600=2 at 37℃ | + | |
- | # Washed | + | High Copy ReceiverとMedium Copy Receiverのディレイタイムはfollowing procedureによってanalyzeした。 |
- | # Mixed them. (Sender:Receiver=1000μL:1000μL) | + | |
- | # Incubated at 30°C. | + | #Transformed sender(Ptet-LuxI), high copy receiver(Ptet-LuxR-Plux-GFP-colE1) and Medium copy receiver(Ptet-LuxR-Plux-GFP-p15A) respectively into E coli strains(BD⊿FliC). |
- | # Measured intensity of green fluorescence at regular time intervals. | + | #Inoculated them independently in liquid media. Incubated at 37℃ 12h. |
+ | #Inoculated again in Fresh liquid media upto about OD600=2 at 37℃ | ||
+ | #Washed sender and receivers. | ||
+ | #Mixed them. (Sender:Receiver=1000μL:1000μL) | ||
+ | #Incubated at 30°C. | ||
+ | #Measured intensity of green fluorescence at regular time intervals.(Fluoroskan AscentR FL&Fluoroskan AscentR Thermo ELECTRON CORPORATION) | ||
===Result=== | ===Result=== | ||
+ | |||
+ | '''>[[Team:Chiba/Project#Receiver|Back to the project page]]''' | ||
{| style="color:white;background-color:Maroon" cellpadding="3" cellspacing="3" border="1" bordercolor="white" width="100%" align="center" | {| style="color:white;background-color:Maroon" cellpadding="3" cellspacing="3" border="1" bordercolor="white" width="100%" align="center" |
Latest revision as of 19:28, 29 October 2008
Home | The Team | The Project | Parts Submitted to the Registry | Reference | Notebook | Acknowledgements |
---|
Contents |
Receiver crosstalk
Design
センダーとレシーバーを元来とは異なる組み合わせにすることによって、thresholdに達する時間を遅くする。(杉山)
Method
Result
Change Receiver's Copy Number
Design
レシーバーのコピーナンバーを減らすことで、thresholdに達するまでの時間を伸ばす。 (小林)
Method
- High Copy Receiver[http://partsregistry.org/Part:BBa_T9002 BBa_T9002 (AHL Reporter)]
- Medium Copy Receiver
High Copy ReceiverとMedium Copy Receiverのディレイタイムはfollowing procedureによってanalyzeした。
- Transformed sender(Ptet-LuxI), high copy receiver(Ptet-LuxR-Plux-GFP-colE1) and Medium copy receiver(Ptet-LuxR-Plux-GFP-p15A) respectively into E coli strains(BD⊿FliC).
- Inoculated them independently in liquid media. Incubated at 37℃ 12h.
- Inoculated again in Fresh liquid media upto about OD600=2 at 37℃
- Washed sender and receivers.
- Mixed them. (Sender:Receiver=1000μL:1000μL)
- Incubated at 30°C.
- Measured intensity of green fluorescence at regular time intervals.(Fluoroskan AscentR FL&Fluoroskan AscentR Thermo ELECTRON CORPORATION)
Result
Home | The Team | The Project | Parts Submitted to the Registry | Notebook |
---|