Difference between revisions of "Part:BBa K1709002:Experience"
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Further DNA sequencing proved the correct sequence, as designed. </p> | Further DNA sequencing proved the correct sequence, as designed. </p> | ||
| + | [[File:RBS-CheZ seq.JPG|500px|center|]] | ||
| + | Part of the sequence alignment with on top the reference sequence and on the bottom the sequencing results.<br/><br/> | ||
[[File:KU_Leuven_GelPurification.jpeg|500px|center|]] | [[File:KU_Leuven_GelPurification.jpeg|500px|center|]] | ||
Latest revision as of 16:13, 26 September 2015
The sequence was verified by restriction mapping and PCR and the presence of colonies expressing GFP proves that the plasmid was designed and cloned correctly.
Further DNA sequencing proved the correct sequence, as designed.
To characterize the CheZ-GFP BioBrick, the fragment containing a RBS was cloned directly after a strong promotor (BBa_J23101). The first figure shows the gel right before ligation.
The colonies were checked by restriction mapping using BcuI and PstI (results not shown). The DNA sequence was also confirmed by DNA sequencing. Results can be provided by email. The presence of colonies expressing GFP proves that the plasmid was designed and cloned correctly.
Further DNA sequencing proved the correct sequence, as designed.
Part of the sequence alignment with on top the reference sequence and on the bottom the sequencing results.
Gel after purification. Lanes 2-5: insert (1400bp). Lane 6: linearized vector. Lanes 7-10 : insert. Lane 11: linearized vector
GFP is expressed in the cells. This confirms the correct construction of the BioBrick
Further characterization could be done by transforming the cheZ knockout Keio strain with this plasmid. These cells should then regain their possibility to swim.
Applications of BBa_K1709002
Motility control
User Reviews
UNIQ588245ab51dfdd15-partinfo-00000000-QINU
UNIQ588245ab51dfdd15-partinfo-00000001-QINU