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Team:University of Alberta/Plant Project
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<h2>'''Back to [https://2008.igem.org/Team:The_University_of_Alberta/Project the projects page].'''</h2> | <h2>'''Back to [https://2008.igem.org/Team:The_University_of_Alberta/Project the projects page].'''</h2> | ||
| + | ==Status of Project== | ||
| + | Currently we have the multiple cloning site (MCS) and the vector that we are introducing it into (p0380). We have optimized the vector p0380 using site directed mutagenesis to remove all pre-existing notI sites from the vector. At the moment we are in the process of verifying that our MCS has been successfully inserted into the vector. | ||
Revision as of 16:25, 28 October 2008
First Seed Pod of the project
Contents |
IGEM's First Binary Vector
Our Binary Vector is a modified pCambia 0380 binary vector link We have added in our own poly linker which includes the proper prefix, suffix and primers to coincide with the IGEM regulations. We also added a CAM resistance cassette.
The First Plant Project Ever Submitted to IGEM
We hope to demonstrate that using biobricks in plants is not only useful but feasible in the restraints of this competition. We also hope to use the tools that we make to insert our toxin detection vector into plants.
Plant Protocol
Growing Plants
Selection of Primary Transformants
Transformation Protocol
Time line
A new tray of plants will be planted every week.
Week 1(Before Biobricks Arrive)
PCR our the resistance gene and promoter from the Pcambia vector
Use Site directed mutagenesis to remove NOTI sites from the vector
Week 2(biobricks have arrived)
Digest new biobrick and confirm it is what it is.
Insert Plant biobrick into the pCambia vector that has had the NOTI sites removed
Transform Vector into Agrobacterium
Confirm Transformation
Create bulk culture of Agrobacterium for plant transformation
Week 3
Transform Plants ( That are 3 weeks old)
Make another bulk culture for next weeks transformation
Week 4-6
Keep transforming plants on tray every week to increase chances.
Harvest seeds of transformed plants and replant them.(continue as seeds come into maturity)
Week 6-End
select for homozygous plants
Back to the projects page.
Status of Project
Currently we have the multiple cloning site (MCS) and the vector that we are introducing it into (p0380). We have optimized the vector p0380 using site directed mutagenesis to remove all pre-existing notI sites from the vector. At the moment we are in the process of verifying that our MCS has been successfully inserted into the vector.
