Difference between revisions of "Part:BBa K274004:Experience"
(→Characterisation by NCTU_FORMOSA) |
|||
| Line 31: | Line 31: | ||
We mutated the sequence to correct the Xba I restriction site . | We mutated the sequence to correct the Xba I restriction site . | ||
| + | |||
| + | And the sequence is made of vioABDE not vioABDE | ||
Revision as of 11:46, 29 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_K274004
User Reviews
UNIQ6cfe460378460266-partinfo-00000000-QINU UNIQ6cfe460378460266-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.
Characterisation by NCTU_FORMOSA
This plasmid did not cut with Xba I restriction site in our hands. As such we could not use it to assemble after other parts.
We mutated the sequence to correct the Xba I restriction site .
And the sequence is made of vioABDE not vioABDE