Difference between revisions of "Part:BBa K274004:Experience"
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When digested with BamHI and NotI, the insert did not digest as expected, only a 2kb band (backbone) and ~6kb band were visible. | When digested with BamHI and NotI, the insert did not digest as expected, only a 2kb band (backbone) and ~6kb band were visible. | ||
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| + | Agree with Team NCTU-Formosa. I wanted to clone vioC from 3-20J, 3-22F, 4-18C in 2011 distribution, all designated as Part BBa-K274004, but the sequencing results showed that they are actually vioABDE. | ||
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| + | Zhenrun Zhang, 'Peking_R iGEM 2011' | ||
== '''Characterisation by 2011 iGEM NCTU_FORMOSA''' == | == '''Characterisation by 2011 iGEM NCTU_FORMOSA''' == | ||
Revision as of 04:35, 5 December 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_K274004
User Reviews
UNIQ1932be48fd3ca1c3-partinfo-00000000-QINU UNIQ1932be48fd3ca1c3-partinfo-00000001-QINU
E.coli turned dark green after transformation of this plasmid, it is not supposed to be so since there is no promoter upstream of the operon. We have not found the reason.
Karina Arnesen, undergraduate, Alberta iGEM 2010
When digested with BamHI and NotI, the insert did not digest as expected, only a 2kb band (backbone) and ~6kb band were visible.
Agree with Team NCTU-Formosa. I wanted to clone vioC from 3-20J, 3-22F, 4-18C in 2011 distribution, all designated as Part BBa-K274004, but the sequencing results showed that they are actually vioABDE.
Zhenrun Zhang, 'Peking_R iGEM 2011'
Characterisation by 2011 iGEM NCTU_FORMOSA
We found out that there's a point mutation in this plasmid. This mutation occurs in the Xba I restriction site which takes a lot of time for us just to digest it in order to ligase this part with our interest part.
The following figure shows the unsual gel electrophoresis result which the Xba I restriction site couldn't recognize the restriction site.
Figure.1 Compare our part before and after digestion to show the point mutation of Xba I.
In order to correct the mutation, we then design a primer as follows:
Figure.2 Design a primer to correct the point mutation.
This primer include the precise sequence of the Xba I restriction site. We then do Polymerase Chain Reaction to extend the remaining sequence and amplify the exact plasmid that we want.
Figure.3 Compare our part before and after digestion to show we correct the mutation successfully
Last and the most important, we also notice something that this part is actually vioABDE instead of vioABCE.
In previous time, we failed in every attempts to clone out vioC from this part. We then decided to do DNA sequencing to make sure every single sequence is correct. Afterward, we found the exact sequence of vioABDE instead of vioABCE.
Please refer to the file for the result of sequencing :Sequencing rev. and Sequencing analysis