Team:HKU-Hong Kong/Parts

From 2011.igem.org

(Difference between revisions)
Line 3: Line 3:
|style="font-family: georgia, helvetica, arial, sans-serif;font-size:2em;color:#01DF01;"|Sample Data Page
|style="font-family: georgia, helvetica, arial, sans-serif;font-size:2em;color:#01DF01;"|Sample Data Page
|-
|-
-
|style="width:900px;"|
+
|style="width:700px;"|
<div ALIGN=CENTER>
<div ALIGN=CENTER>
  {| style="width:800px;background:#99EE63;text-align:center;font-family: georgia, helvetica, arial, sans-serif;color:#000000;margin- top:5px;padding: 2px;" cellspacing="5";
  {| style="width:800px;background:#99EE63;text-align:center;font-family: georgia, helvetica, arial, sans-serif;color:#000000;margin- top:5px;padding: 2px;" cellspacing="5";

Revision as of 14:30, 5 October 2011

Sample Data Page
Sample Data Parts.png

By expressing the tetR:H-NS fusion proteins, the tetR part of the proteins wound recognize and specifically bind to the tetR binding region (tetO2). There are two tet-R binding sites as tet-R form a dimer as in the tet repressor- operator system. As the fusion proteins bound to tet-O, it is expected that the H-NS part of the fusion protein would attract and oligomerize with other native H-NS proteins inside the cell. With the oligomerization of the fusion proteins and native H-NS, the DNA covered by the oligomers is expected to trap the RNA polymerase during transcription, thus gene (GFP) repression is achieved.


Parts that we have created:

(The favorite parts are selected based on the potential to be used in our Super silencer repression system)

Click here to take the tour...