"
Team:Alberta
From 2012.igem.org
Rick24568509 (Talk | contribs) |
Rick24568509 (Talk | contribs) |
||
| Line 16: | Line 16: | ||
<html> | <html> | ||
<div class="underline"> | <div class="underline"> | ||
| - | <font size= | + | <font size=4> |
Abstract | Abstract | ||
</font> | </font> | ||
| Line 29: | Line 29: | ||
<html> | <html> | ||
<div class="underline"> | <div class="underline"> | ||
| - | <font size= | + | <font size=4> |
Finished work | Finished work | ||
</font> | </font> | ||
| Line 58: | Line 58: | ||
<html> | <html> | ||
<div class="roundBox"> | <div class="roundBox"> | ||
| - | <font size= | + | <font size=4> |
2012 Sponsors | 2012 Sponsors | ||
</font> | </font> | ||
Revision as of 17:56, 10 September 2012
|
|
Welcome to the 2012 Alberta iGEM team Wiki!
This wiki is still under construction, and as such may contain missing pages or information. Do not grieve, we are still working on expanding it.
As a young team composed of high schoolers and junior undergraduates, we selected a project aimed at giving ourselves a firm understanding in the fundamentals of genetic engineering and control. The end goal of our project was to create spatial color patterns using bacteria, such as a color wheel and a rainbow, that required control over several color outputs in response to spatial gradients of chemical inducers. Colour gradients were achieved using a high-copy plasmid that contained both an inducible colour gene and its corresponding repressor. Colour banding was achieved by a novel means of adjusting gene expression through plasmid copy number control that varied from 0 to ~1000 copies/cell as a function of inducer concentration. Note that the rapid loss of plasmid that occurs in the absence of inducer also constitutes a novel and extremely effective safety switch for genetically engineered organisms which might enter the environment.
description
description
