Team:Missouri Miners

From 2011.igem.org

(Difference between revisions)
Line 1: Line 1:
-
{| style="color:#006400; background-color:#7fff00;" cellpadding="3" cellspacing="1" border="3px solid" bordercolor="#006400" width="62%" align="center"
+
{| style="color:#006400; background-color:#eac117;" cellpadding="3" cellspacing="1" border="0px solid" bordercolor="#006400" width="100%" align="center"
!align="center"|[[Team:Missouri_Miners|Home]]
!align="center"|[[Team:Missouri_Miners|Home]]
!align="center"|[[Team:Missouri_Miners/Team|Team]]
!align="center"|[[Team:Missouri_Miners/Team|Team]]
Line 11: Line 11:
|}
|}
<html>
<html>
-
<div id="box" style="width: 850px; margin-left: 50px; padding: 5px; border: 3px solid #000; background-color: #7fff00;">
+
<div id="box" style="width: 850px; margin-left: 40px; padding: 5px; border: 15px solid #006400; background-color: #c0c0c0;">
-
<div id="template" style="text-align: center; font-weight: bold; font-size: large; color: black; padding: 5px;">
+
<div id="template" style="text-align: center; font-weight: bold; font-size: large; color: #006400; padding: 5px;">
Project Summary
Project Summary
</div>
</div>
-
<div id="instructions" style="text-align: center; font-weight: bold; font-size: small; color: #006400; padding: 5px;">
+
<div id="instructions" style="text-align: center; font-weight: bold; font-size: small; color: black; padding: 5px;">
We are attempting to integrate a glucose controlled promoter gene (Omp-R) linked to a green flousecence producing gene (eYFP) in order to measure the concentration of glucose recquired to activate the promoter gene. Once this concentration is known, we will be attempting to mutate the Omp-R promoter gene so that it will be activated by glucose concentrations closer to those of the average human.
We are attempting to integrate a glucose controlled promoter gene (Omp-R) linked to a green flousecence producing gene (eYFP) in order to measure the concentration of glucose recquired to activate the promoter gene. Once this concentration is known, we will be attempting to mutate the Omp-R promoter gene so that it will be activated by glucose concentrations closer to those of the average human.
</div>
</div>
Line 21: Line 21:
</html>
</html>
-
<div id="box" style="width: 850px; margin-left: 50px; padding: 5px; border: 3px solid #000; background-color: #7fff00;">
+
<div id="box" style="width: 850px; margin-left: 40px; padding: 5px; border: 15px solid #006400; background-color: #c0c0c0;">
-
<div style="text-align: left; font-weight: normal; font-size: normal; color: #006400; padding: 5px;">
+
<div style="text-align: left; font-weight: normal; font-size: normal; color: black; padding: 5px;">
<div style=" font-weight: bold; font-size:large; color: black">  
<div style=" font-weight: bold; font-size:large; color: black">  
<i>Instructors:</i>  
<i>Instructors:</i>  
</div>
</div>
-
<div style=" font-weight: bold; font-size: large">
+
<div style=" font-weight: bold; font-size: large; color: #006400">
Dr. David Westenberg:
Dr. David Westenberg:
</div>
</div>
Line 47: Line 47:
</p>
</p>
-
<div style=" font-weight: bold; font-size: large">
+
<div style=" font-weight: bold; font-size: large; color: #006400">
Dr. Katie Shannon
Dr. Katie Shannon
</div>
</div>

Revision as of 01:10, 17 July 2011

Home Team Official Team Profile Project Parts Submitted to the Registry Modeling Notebook Safety Attributions

Project Summary
We are attempting to integrate a glucose controlled promoter gene (Omp-R) linked to a green flousecence producing gene (eYFP) in order to measure the concentration of glucose recquired to activate the promoter gene. Once this concentration is known, we will be attempting to mutate the Omp-R promoter gene so that it will be activated by glucose concentrations closer to those of the average human.

Instructors:

Dr. David Westenberg:

Prof,Asoc of Biological Sciences

Education:

University of CA - Los Angeles, Doctor of Philosophy, 1991

Research Interests:

  • Regulation of the bradyrhizobium japonicum sdh operon encoding succinate dehydrogenase
  • Evidence for AHL autoinducer production by the soybean symbiont bradyrhizobium japonicum
  • High efficiency separation of microbial aggregates using capillary electrophoresis
  • separating microbes in the manner of molecules. 1. Capillary electrokinetic approaches
  • Succinate dehydrogenase (Sdh) from Bradyrhizobium japonicum is closely related to mitochondrial Sdh

Dr. Katie Shannon

Prof, Ast or Biological Sciences

Education:

Harvard Medical School, Doctor of Philosophy, 2000

Research Interests:

  • Cytokinesis
  • Cell Cycle
  • Cytoskeleton
  • Nanoparticle uptake and transport