Team:Washington/Parts

From 2011.igem.org

(Difference between revisions)
Line 4: Line 4:
<center><big><big><big><big>Data Page</big></big></big></big></center><br><br>
<center><big><big><big><big>Data Page</big></big></big></big></center><br><br>
-
<gallery caption="An Overview of the 2011 UW iGEM Teams Summer Projects" widths="435px" heights="400px" perrow="2">
+
<gallery caption="An Overview of the 2011 UW iGEM Teams Summer Projects" widths="300px" heights="400px" perrow="3">
-
Image:Diesel Production for Wiki 2.png|<left>'''Make It:  Diesel Production'''<br>Insert brief explanation of figure above here</center>
+
Image:Diesel Production for Wiki 2.png||left|'''Make It:  Diesel Production'''<br>Insert brief explanation of figure above here
-
Image:Gluten Destruction for Wiki.png|<center>'''Break It:  Gluten Destruction'''<br>Insert brief explanation of figure above here</center>
+
Image:Gluten Destruction for Wiki.png|center'''Break It:  Gluten Destruction'''<br>Insert brief explanation of figure above here
-
Image:Gibson Assembly and Magnetosomes for Wiki.png|<right>'''The GibsonBricks ToolKit'''<br>Insert brief explanation of figure above here</center>
+
Image:Gibson Assembly and Magnetosomes for Wiki.png|right'''The GibsonBricks ToolKit'''<br>We completed two iGEM toolkits. In the first we created five Gibson Cloning versions of traditional biobrick vectors, and in the second we cloned the genes essential for magnetosome formation and transformed two into ''E. coli''
</gallery>
</gallery>

Revision as of 02:27, 23 September 2011


Data Page


An Overview of the 2011 UW iGEM Teams Summer Projects

|left|Make It: Diesel Production
Insert brief explanation of figure above here

centerBreak It: Gluten Destruction
Insert brief explanation of figure above here

rightThe GibsonBricks ToolKit
We completed two iGEM toolkits. In the first we created five Gibson Cloning versions of traditional biobrick vectors, and in the second we cloned the genes essential for magnetosome formation and transformed two into E. coli



Data Summary

Data for Favorite New Parts

Fill Me In.. here is an example:

  1. [http://partsregistry.org/Part:BBa_X0X0X Main Page] - BAR responsive promoter, BBa_X0X0X: promoter can be induced to express a marker gene (GFP) when exposed to skunk smell (Butanethiol, C4H9SH), but not when exposed to pleasant scents
  2. [http://partsregistry.org/Part:BBa_XXX00 Main Page] - Insulated Vector, BBa_XXX00: un-induced leaky expression is blocked by transcriptional terminators
  3. [http://partsregistry.org/Part:BBa_000XX Main Page] - BAR Bad Odor Receptor, BBa_000XX: yellow fluorescent protein-tagged BAR (BBa_X00XX) shows that BAR is produced in E. coli


Data for Existing Parts

Fill Me In

  1. [http://partsregistry.org/Part:BBa_J45119:Experience Experience] - Wintergreen odor enzyme generator, BBa_J45119 (MIT, iGEM 2006): 98 out of 100 volunteer subjects standing up to 5 feet away from the bacterial cultures could distinguish wintergreen-producing bacteria from negative controls.
  2. [http://partsregistry.org/Part:BBa_J61110:Experience Experience] - RBS, BBa_J61110 (Arkin Lab, 2007): Of the 5 RBS Parts we tested, this RBS works best for expressing yellow fluorescent protein-tagged BAR


Improved Parts

Fill Me In

  1. [http://partsregistry.org/Part:BBa_XXXXX Main Page] - Air Freshilizor, BBa_XXXXX: Our mathematical model predicts that the threshold of activation is 10 parts per billion, the concentration of Butanethiol that humans can typically smell


All Submitted Parts

<groupparts>iGEM011 Washington</groupparts>

Retrieved from "http://2011.igem.org/Team:Washington/Parts"