IGEM:Virginia 2012/Protocols: Difference between revisions
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* [[/Isolating the Phage Genome|Isolating the Phage Genome]] | * [[/Isolating the Phage Genome|Isolating the Phage Genome]] | ||
* [[/CaCl2 Competent Stock Cells | CaCl2 Competent Stock Cells]] | * [[/CaCl2 Competent Stock Cells | CaCl2 Competent Stock Cells]] | ||
* [http://tools.invitrogen.com/content/sfs/manuals/subcloningefficiencydh5alpha_man.pdf Chemical transformation] | |||
* [[/Using the NanoDrop | Using the NanoDrop]] | * [[/Using the NanoDrop | Using the NanoDrop]] | ||
Revision as of 13:09, 4 June 2012
Here is a list of the protocols the 2012 Virginia iGEM team will be following in order to carry out our research project.
Protocols
- Phage Amplification
- Plaque Assay -- to quantify the amount of bacteriophages in our samples.
- Phage Isolation
- Phage Replication Rate Assay
- Preparing a Pertussis Culture
- Isolating the Phage Genome
- CaCl2 Competent Stock Cells
- Chemical transformation
- Using the NanoDrop
Solution & Plate Preparations
- Bordet Gengou (BG) Agar Plate Preparation for culturing B. pertussis.
- LB Broth or Agar Preparation for culturing B. bronchiseptica.
- PEG/NaCl Preparation
- SM Buffer Preparation
- SSM Media Preparation
- TE Buffer
