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Team:Leeds/Parts
From 2013.igem.org
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==Currently Working On== | ==Currently Working On== | ||
| - | + | * Bio-system 1: pCpxR promoter activates GFP expression. Will produce the green fluorescent protein on membrane stress. | |
| - | + | * Bio-system 2: Constitutive genes produce YFP and Ice nucleation protein with a silica binding domain at the c-terminus. | |
| - | + | * Bio-system 3: integration of 1 and 2, INP Si4is constitutively produced but the fluorescent protein is under control of pCpxR promoter. When bound to silica beads will fluoresce | |
| - | + | * Also planning on having the silica binding peptide submitted as its own part for others to use for their own purposes. | |
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==Submitted== | ==Submitted== | ||
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==Characterisation Protocols== | ==Characterisation Protocols== | ||
| - | + | * Bio-system 1: Bacteria exposed to hydrophobic beads to induce membrane stress and fluorescence response is measured using a flourimeter. | |
| - | + | * Bio-system 2: Bacteria exposed to silica beads and washed. Control with no silica binding domain. Those that have bound will be visualised on the beads and those that have not will be seen in the elution. | |
| - | + | * Bio-system 3: Expose the bacteria to silica beads will fluoresce when bound and not fluoresce when unbound. Measure the fluorescence with flourimeter. | |
| - | + | * The Si4 domain will be characterised with bio-system 2 if binding occurs. | |
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Revision as of 15:54, 9 July 2013
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 | Please check back here frequently for a full list of the parts we've developed, submitted to the registry and have had approved. We will also endeavour to include our characeterisation protocols, although we are currently collaborating with Purdue to decide exactly what these should be.
Currently Working On
SubmittedA full listing of all parts Leeds iGEM 2013 have submitted to the Registry, and their status.
Characterisation Protocols
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Everything Below Here To Be Removed
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 all of the pages listed in the menu below with the names specified. PLEASE keep all of your pages within your teams namespace.
| Home | Team | Official Team Profile | Project | Parts Submitted to the Registry | Modeling | Notebook | Safety | Attributions |
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An important aspect of the iGEM competition is the use and creation of standard biological parts. Each team will make new parts during iGEM and will place them in the [http://partsregistry.org Registry of Standard Biological Parts]. The iGEM software provides an easy way to present the parts your team has created . The "groupparts" tag will generate a table with all of the parts that your team adds to your team sandbox. Note that if you want to document a part you need to document it on the [http://partsregistry.org Registry], not on your team wiki.
Remember that the goal of proper part documentation is to describe and define a part such that it can be used without a need to refer to the primary literature. The next iGEM team should be able to read your documentation and be able to use the part successfully. Also, you should provide proper references to acknowledge previous authors and to provide for users who wish to know more.
<groupparts>iGEM013 Leeds</groupparts>
