Difference between revisions of "Part:BBa K292006:Experience"

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<I>NTNU_Trondheim 2011</I>
 
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We found and orderd this part from the parts registry.  
 
We found and orderd this part from the parts registry.  

Revision as of 16:30, 19 September 2011

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_K292006

Reliable to use when we want to control a gene expression by using pLac promoter. In fact when LacI is not expressed, pLac is activated, and when there is an expression of LacI, pLac is inhibited. We can easily design a system to induce the transcription of LacI by using another operon as the tetracycline operon and creates a failed feedback mechanism for pLac inhibition and so, for gene expression inhibition.


User Reviews

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NTNU_Trondheim 2011

We found and orderd this part from the parts registry. Since it had RBS and double terminator it would save us from some cloning work.

When testcutting the constructs containing BBa_K292006 we got some unexpected results. Therefore we decided to digest the brick with three differnt enzymes with restriction sites in the given biobrick-sequence in addition to EcoR1 and PstI (for looking at the biobrick length) Except from the sample cut with EcorR1 and PstI, the samples were also cut with BglI wich has a recognition site in the pSB1A2 backbone.

LacI2 plasmid cut with EcoR1 + PstI, BglI + BclI, BglI + EcoRV, BglI + BanII

Overwiev of restrctions and expected fragmentlengths:

Restriction enzymes Expected lengths (bp)
EcoR1 + PstI 2053 (backbone) and 1303 (biobrick)
BglI + BclI 2032 + 1324
BglI + EcoRV 1760 + 1596
BglI + BanII 1835 + 1521

As we can see on the resulting gel none of the restriction sites inn the LacI2 fragment appear to be present. In additon the LacI2 insert looks smaller than it's supposed to be. This indicates that the biobrick sequence does not match the sequence given in the parts registry.



TetR + p(TetR)+RFP (BBa_K092600) and TetR + p(TetR)+RFP+luxI (BBa_K092700)

At the beginning of the project our ide was to use this TetR regulated system to build the stress sensor. However our experience with the two biobricks is bad. Transformants did not show any signs of fluorescent activity, and the fragment lengths after enzyme digestion were not as expected.

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