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+ | <div id="bioS_what" class="content-div"> | ||
+ | <center><h2>Attributions</h1></center> | ||
+ | <table class="content-layout"> | ||
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+ | <p style="text-align:left;"> | ||
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+ | Team Leader: Jessica Birt | ||
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+ | Experimental: Valeria Verrone (Head) | ||
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+ | IPTG Sensor: Declan Kohl, Jessica Birt | ||
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+ | Arsenic Biosensor: Valeria Verrone, Declan Kohl | ||
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+ | Sarcosine Oxidase: Sophie Badger | ||
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+ | FimE Switch: Marcia Pryce | ||
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+ | Cell Free System: Bradley Brown | ||
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+ | deGFP: Sophie Badger, Bradley Brown, Lais Takiguchi | ||
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+ | Chromoproteins: Sophie Badger, Lais Takiguchi | ||
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+ | Processing Variants: Jessica Birt, Marcia Pryce, Lais Takiguchi | ||
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+ | Synthetic Promoter Library: Lais Takiguchi | ||
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+ | Fluorescene Normalisation: Michaela Chapman, Ansh Vyas | ||
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+ | Assembly Methods: Anna Walsh, Michaela Chapman, Evie Whittaker | ||
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+ | Microfluidics: Jack Cooper | ||
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+ | Robotics: Jessica Birt, Declan Kohl | ||
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+ | Interlab: Michaela Chapman (Head), Declan Kohl, Zoe Wilson, Marcia Pryce, Ansh Vyas | ||
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+ | Human Practices: Declan Kohl (Head), Zoe Wilson, Jessica Birt | ||
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+ | Integrated: Declan Kohl, Jessica Birt | ||
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+ | Outreach and Education: Declan Kohl, Zoe Wilson, Sophie Badger, Marcia Pryce | ||
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+ | Scientific Communication Analysis: Zoe Wilson<br /> | ||
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+ | Modelling: Jessica Birt (Head), Bradley Brown | ||
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+ | Simbiotics: Jessica Birt | ||
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+ | Design of Experiment: Bradley Brown | ||
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+ | Wiki: Marcia Pryce (Head), Bradley Brown, Jack Cooper, Declan Kohl | ||
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+ | Poster Development: All Team Members | ||
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+ | Presentation Development: All Team Members | ||
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+ | Presenters: Declan Kohl | ||
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+ | </p> | ||
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+ | <!--------------- | ||
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+ | <div style="width:600px; background-color:#efffff"> | ||
+ | <img width="100%" src="https://static.igem.org/mediawiki/2017/6/6b/T--Newcastle--BB_project_overview.png"> | ||
+ | </div> | ||
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+ | <p style="background-color:#efffff"> | ||
+ | We aim to produce a toolbox that can be used to construct biosensors. This toolbox will contain devices which can be used to construct biosensors. As the toolbox will contain various devices, as well as chassis, several properties and functionalities for biosensors are possible. To assist with design and development the toolbox will contain in silico tools.<br /> | ||
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+ | We also aim to develop a biosensor development technique which allows easy and rapid development and testing of biosensor variants. Each device in our toolbox can be expressed in a separate cell and co-cultured with other cells expressing different devices to produce a functional biosensor. For example, three cell strains expressing an inducible promoter (detector device), a signal amplification device (processing device), and a fluorescent protein (reporter device) can be co-cultured together to make a biosensor. Devices in each cell will communicate through the use of 'connectors', which take the form of quorum sensing molecules.<br /> | ||
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+ | To surpass beyond the lab we want to contribute to the biological community. We aim to highlight the need for our toolbox, by conducting an investigation into the progression of biosensors from research to distribution, as well as the availability of and demand for biosensors. How often biosensors successfully progress from design to distribution, and identification of and issues encountered at each stage of this progression will be investigated, and the results implemented into the toolbox, aiming to help overcome these issues. | ||
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Revision as of 10:06, 6 September 2017
Attributions
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