Team:Washington/Tools Created/New Vectors

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'''&larr; [[Team:Washington/Project/Tools/Klavins|Next-Gen Cloning]]'''
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Revision as of 18:12, 27 September 2010

Protien Expression Vectors

As part of the protien expression process in the gram positive theraputics portion

Vector Design

Vector

f1 origin

Lac I

Promoters

link to the 4 BBa parts

Ribosome Binding Site

link to bba b0034

Building the Vectors

overview of what was done in one paragraph... links to protocols used (need to put up pcr (taq/fusion) digestion, ligation, transformation links to registry)


Testing the Vectors

Protien Expression

The vector cassette was placed in 4 different plasmid backbone from the registry(psb1c3, psb1a3, psb3k3, psb4a5.. make into links) and GFP (BBa E0040) was placed in the protein expression area of the vector. Data was pulled and expressed below....

Placeholder...

f1 origin

The f1 origin was tested by compairing infected verse none infected DNA isolation amounts (explain in more detail once this is done)

Placeholder...


Next-Gen Cloning       Safety Information