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Team:Princeton/Experiments
From 2008.igem.org
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{{PrincetonHeader}} | {{PrincetonHeader}} | ||
| - | + | ==Bio-brick Creation== | |
'''Lab Protocols''' | '''Lab Protocols''' | ||
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| - | 1. Primer Design | + | |1. Primer Design |
2. [[PCR Amplification]] | 2. [[PCR Amplification]] | ||
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7. [[PCR Purification]] | 7. [[PCR Purification]] | ||
| - | 8. [[Ligate DNA]] | + | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||| |
| + | |8. [[Ligate DNA]] | ||
9. [[Transformation and Plating]] | 9. [[Transformation and Plating]] | ||
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14. [[Sequence]] | 14. [[Sequence]] | ||
| + | |} | ||
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| - | + | ==Bio-Brick Verification== | |
'''Cell Culture Process''' | '''Cell Culture Process''' | ||
Latest revision as of 07:57, 29 October 2008
PRINCETON IGEM 2008
| Home | Project Overview | Project Details | Experiments | Results | Notebook |
|---|
| Parts Submitted to the Registry | Modeling | The Team | Gallery |
|---|
Bio-brick Creation
Lab Protocols
| 1. Primer Design
4. PCR SOEing 5. Digestion | 8. Ligate DNA
11. Restriction Map/ Restriction Digest 12. Re-transform with selected plasmid 13. Extract DNA (Maxiprep or Midiprep) 14. Sequence |
Bio-Brick Verification
Cell Culture Process
3. Infection
Also,
