IGEM:Virginia 2012/Protocols

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(Protocols)
Current revision (17:42, 2 October 2012) (view source)
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==Protocols==
==Protocols==
* [[/Phage Amplification|Phage Amplification]]
* [[/Phage Amplification|Phage Amplification]]
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* [[/Plaque Assay|Plaque Assay]] -- to quantify the amount of bacteriophages in our samples.
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* [[/Plaque Assay|Plaque Assay]] -- to quantify the amount of bacteriophage in a sample.
* [[/Phage Isolation|Phage Isolation]]
* [[/Phage Isolation|Phage Isolation]]
* [[/Phage Replication Rate Assay|Phage Replication Rate Assay]]
* [[/Phage Replication Rate Assay|Phage Replication Rate Assay]]
* [[/Preparing a Pertussis Culture|Preparing a Pertussis Culture]]
* [[/Preparing a Pertussis Culture|Preparing a Pertussis Culture]]
* [[/Isolating the Phage Genome|Isolating the Phage Genome]]
* [[/Isolating the Phage Genome|Isolating the Phage Genome]]
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* [[/CaCl2 Competent Stock Cells | CaCl2 Competent Stock Cells]]
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* [http://tools.invitrogen.com/content/sfs/manuals/subcloningefficiencydh5alpha_man.pdf Chemical transformation]
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* [[/Using the NanoDrop | Using the NanoDrop]]
==Solution & Plate Preparations==
==Solution & Plate Preparations==
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* [[/SM Buffer Preparation|SM Buffer Preparation]]
* [[/SM Buffer Preparation|SM Buffer Preparation]]
* [[/SSM Media Preparation|SSM Media Preparation]]
* [[/SSM Media Preparation|SSM Media Preparation]]
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* [http://en.wikipedia.org/wiki/TE_buffer TE Buffer]

Current revision

Here is a list of the protocols the 2012 Virginia iGEM team will be following in order to carry out our research project.

Protocols

Solution & Plate Preparations

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