Team:Washington/Magnetosomes/Future

From 2011.igem.org

(Difference between revisions)
(→Future Direction)
Line 4: Line 4:
==Future Direction==
==Future Direction==
 +
We will keep working on adding more components into the toolkits at UW and hope that future iGEM teams will be able to use toolkits to join in on the fun!
As mentioned in the introduction, the purpose of this part of the project is to bring cloning from single gene level to multi-genes level to increase the complexity of the circuit that can possibly be constructed.....  
As mentioned in the introduction, the purpose of this part of the project is to bring cloning from single gene level to multi-genes level to increase the complexity of the circuit that can possibly be constructed.....  
 +
-----
 +
<br/>
 +
;Gibson Vector
 +
We have developed and submitted several vectors that are Gibson Cloning friendly(see the "parts submitted" page). More of such vectors should be developed and added to the toolkit in the future.
-
1) Gibson Vector
+
;Magnetosome Project
-
We have developed and submitted several vectors that are Gibson Cloning friendly(see the "parts submitted" page). More of such vectors should be developed in the future...
+
We still have a long way to achieve our goal of making magnetic ''E.colo'' but this project is certainly worth investigating. We have a ton of project ideas for the future teams...
-
 
+
<br/>
-
2) Magnetosome Project:
+
*Express the rest of the gene in the MAI region in E.coli
-
The ability to produce and control uniform, nano-sized magnetic particles is attractive in areas such as medical imaging and nano-electronics where scientists and engineers are actively seeking innovative solutions for breakthrough in size and accuracy. Thus this project is worth continuing  and we propose the following to be done in the future....
+
*Co-express the genes and study their interaction
-
 
+
*Build the scaffold structure in E.coli
-
-Express the rest of the gene in the MAI region in E.coli
+
*Express the full assembly in E.coli
-
-Co-express the genes and study their interaction
+
*Develop assay for the magnet formation
-
-Build the scaffold structure in E.coli
+
*Determine the optimal cell growth condition......
-
-Express the full assembly in E.coli
+
-
-Develop assay for the magnet formation?
+

Revision as of 20:49, 22 September 2011


Future Direction

We will keep working on adding more components into the toolkits at UW and hope that future iGEM teams will be able to use toolkits to join in on the fun! As mentioned in the introduction, the purpose of this part of the project is to bring cloning from single gene level to multi-genes level to increase the complexity of the circuit that can possibly be constructed.....


Gibson Vector

We have developed and submitted several vectors that are Gibson Cloning friendly(see the "parts submitted" page). More of such vectors should be developed and added to the toolkit in the future.

Magnetosome Project

We still have a long way to achieve our goal of making magnetic E.colo but this project is certainly worth investigating. We have a ton of project ideas for the future teams...

  • Express the rest of the gene in the MAI region in E.coli
  • Co-express the genes and study their interaction
  • Build the scaffold structure in E.coli
  • Express the full assembly in E.coli
  • Develop assay for the magnet formation
  • Determine the optimal cell growth condition......
Retrieved from "http://2011.igem.org/Team:Washington/Magnetosomes/Future"