Difference between revisions of "Part:pSB1C3:Experience"

 
(→‎User Reviews)
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
 
This experience page is provided so that any user may enter their experience using this part.<BR>Please enter
Line 18: Line 17:
 
|};
 
|};
 
<!-- End of the user review template -->
 
<!-- End of the user review template -->
 +
<!-- DON'T DELETE --><partinfo>pSB1C3 EndReviews</partinfo>
 +
 +
<!-- DON'T DELETE --><partinfo>pSB1C3 StartReviews</partinfo>
 +
<!-- Template for a user review
 +
{|width='80%' style='border:1px solid gray'
 +
|-
 +
|width='10%'|
 +
<partinfo>pSB1C3 AddReview 1</partinfo>
 +
<I>Username</I>
 +
|width='60%' valign='top'|
 +
Enter the review inofrmation here.
 +
|};
 +
<!-- End of the user review template -->
 +
{|width='80%' style='border:1px solid gray'
 +
|-
 +
|width='10%'|
 +
<partinfo>pSB1C3 AddReview 5</partinfo>
 +
<I>UNIPV-Pavia iGEM 2011</I>
 +
|width='60%' valign='top'|
 +
<html>
 +
 +
This cloning vector has been improved, cloning in it the strong p<sub>Tet</sub> promoter, between E and X restriction sites; the mRFP coding sequence from BBa_J61002, has been placed between S and P restirction sites, in order to facilitate the cloning of coding sequences downstream p<sub>Tet</sub> promoter in this high cpy number plasmid.<br>
 +
For more details see the <a = href="https://parts.igem.org/Part:BBa_K516999:Experience#expPV11">BBa_K516999 experience page</a>.
 +
 +
</html>
 +
|}
 +
 +
 
<!-- DON'T DELETE --><partinfo>pSB1C3 EndReviews</partinfo>
 
<!-- DON'T DELETE --><partinfo>pSB1C3 EndReviews</partinfo>

Revision as of 19:27, 23 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 pSB1C3

User Reviews

UNIQe41c389c408cc6bd-partinfo-00000000-QINU UNIQe41c389c408cc6bd-partinfo-00000001-QINU

UNIQe41c389c408cc6bd-partinfo-00000002-QINU

•••••

UNIPV-Pavia iGEM 2011

This cloning vector has been improved, cloning in it the strong pTet promoter, between E and X restriction sites; the mRFP coding sequence from BBa_J61002, has been placed between S and P restirction sites, in order to facilitate the cloning of coding sequences downstream pTet promoter in this high cpy number plasmid.
For more details see the BBa_K516999 experience page.


UNIQe41c389c408cc6bd-partinfo-00000005-QINU