Difference between revisions of "Part:BBa K1709003:Experience"

Line 1: Line 1:
 
__NOTOC__
 
__NOTOC__
This experience page is provided so that any user may enter their experience using this part.<BR>Please enter
 
how you used this part and how it worked out.
 
 
===Applications of BBa_K1709003===
 
 
===User Reviews===
 
<!-- DON'T DELETE --><partinfo>BBa_K1709003 StartReviews</partinfo>
 
<!-- Template for a user review
 
{|width='80%' style='border:1px solid gray'
 
|-
 
|width='10%'|
 
<partinfo>BBa_K1709003 AddReview 5</partinfo>
 
<I>VinnieVD</I>
 
|width='60%' valign='top'|
 
 
|};
 
<!-- End of the user review template -->
 
 
<p>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.<br/>
 
<p>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.<br/>
 
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.<br/>
 
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.<br/>
Line 36: Line 19:
 
<br/>
 
<br/>
 
<br/>
 
<br/>
 +
 +
===Applications of BBa_K1709003===
 +
 +
===User Reviews===
 +
<!-- DON'T DELETE --><partinfo>BBa_K1709003 StartReviews</partinfo>
 +
<!-- Template for a user review
 +
{|width='80%' style='border:1px solid gray'
 +
|-
 +
|width='10%'|
 +
<partinfo>BBa_K1709003 AddReview 5</partinfo>
 +
<I>VinnieVD</I>
 +
|width='60%' valign='top'|
 +
 +
|};
 +
<!-- End of the user review template -->
 +
 
<!-- DON'T DELETE --><partinfo>BBa_K1709003 EndReviews</partinfo>
 
<!-- DON'T DELETE --><partinfo>BBa_K1709003 EndReviews</partinfo>

Revision as of 14:59, 26 September 2015

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.


KU Leuven GelPurification.jpeg

Gel after purification. Lanes 2-5: insert (1400bp). Lane 6: linearized vector. Lanes 7-10 : insert. Lane 11: linearized vector


KU Leuven fluorescence.jpg

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_K1709003

User Reviews

UNIQ4919ff193fe28f81-partinfo-00000000-QINU

UNIQ4919ff193fe28f81-partinfo-00000001-QINU