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Team:Baltimore/Project
From 2011.igem.org
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| + | TEAM BALTIMORE'S ABSTRACT | ||
| + | Our Goal is to provide a way for anyone to be able to make their own Taq polymerase instead of having to purchase it. However, the gene for Taq polymerase has a PstI site located within the coding sequence which makes it incompatible with the BioBrick assembly standard. In order to make the Taq polymerase compatible with the BioBrick assembly standard we need to change the sequence through site directed mutagenesis in a way that would maintain the amino acid sequence of the protein but change the DNA sequence of the gene. | ||
== Project Details== | == Project Details== | ||
Revision as of 21:01, 7 July 2011
This is a template page. READ THESE INSTRUCTIONS.
You are provided with this team page template with which to start the iGEM season. You may choose to personalize it to fit your team but keep the same "look." Or you may choose to take your team wiki to a different level and design your own wiki. You can find some examples HERE.
You MUST have a team description page, a project abstract, a complete project description, a lab notebook, and a safety page. PLEASE keep all of your pages within your teams namespace.
| You can write a background of your team here. Give us a background of your team, the members, etc. Or tell us more about something of your choosing. | File:Baltimore logo.png 200px |
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Tell us more about your project. Give us background. Use this is the abstract of your project. Be descriptive but concise (1-2 paragraphs) | File:Baltimore team.png Your team picture |
| Team Example |
| Home | Team | Official Team Profile | Project | Parts Submitted to the Registry | Modeling | Notebook | Safety | Attributions |
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TEAM BALTIMORE'S ABSTRACT
Our Goal is to provide a way for anyone to be able to make their own Taq polymerase instead of having to purchase it. However, the gene for Taq polymerase has a PstI site located within the coding sequence which makes it incompatible with the BioBrick assembly standard. In order to make the Taq polymerase compatible with the BioBrick assembly standard we need to change the sequence through site directed mutagenesis in a way that would maintain the amino acid sequence of the protein but change the DNA sequence of the gene.
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