Difference between revisions of "Part:BBa J09855:Experience"

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This part is tested by 2012 iGEM team '''Tsinghua.'''
 
This part is tested by 2012 iGEM team '''Tsinghua.'''
  
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To tell the truth, when we use this part for the first time, it didn't work well. Then we sequenced the part using prefix and suffix primer. We found that there are some part missed in Plac promoter at the beginning and in Plux promoter at the end. So we rebuilt this part and modified for a little. This modification improve the efficiency of transcription. The sequensing results show that our construct is correct.
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To tell the truth, when we use this part for the first time, it didn't work well. Then we sequenced the part using prefix and suffix primer. We found that there are some part missed in Plac promoter at the beginning and in Plux promoter at the end. Maybe this is why it can't work.
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We improve this part and modify sequence. We add several nucleic acid to the Plac promoter and plux promoter. This modification improve the efficiency of transcription. The sequensing results show that our construct is correct.

Revision as of 13:05, 26 September 2012

This experience page is provided so that any user may enter their experience using this part.
Please enter how you used this part and how it worked out.

Applications of BBa_J09855

This part is tested by 2012 iGEM team Tsinghua.

We use this part to work as a promoter system which can be activated by C6HSL. We can add some other gene dowmstream so that AHL can work as a signal. In our project this year, we use this part and modified it to get more complicated construct.

User Reviews

UNIQcb790205444437e8-partinfo-00000000-QINU UNIQcb790205444437e8-partinfo-00000001-QINU This part is tested by 2012 iGEM team Tsinghua.

To tell the truth, when we use this part for the first time, it didn't work well. Then we sequenced the part using prefix and suffix primer. We found that there are some part missed in Plac promoter at the beginning and in Plux promoter at the end. Maybe this is why it can't work.


We improve this part and modify sequence. We add several nucleic acid to the Plac promoter and plux promoter. This modification improve the efficiency of transcription. The sequensing results show that our construct is correct.