Team:Heidelberg

From 2009.igem.org

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<div id="orangeBox"><h3>Design your own promoter</h3>
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<p>As one of the most important approaches to synthezise synthetic promoters we developed a database that predicts the position of conserved promoter binding sequences. We coded an easy to use interface that is available for public use. </p>
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<a href="#">Start Design</a>
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</div>
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<div id="greenBox"><h3>Mission 2009:<br>mammalian biobricks</h3>
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<p>Mammalian synthetic biology has huge potential, but it is in need of new standards and of systematic construction of comprehensive part libraries. Learn more about our new mission on the project page. </p>
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<a href="#">Go To Project Page</a>
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</div>
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<div id="blueBox"><h3>Mission accomplished</h3>
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<p>We developed two novel, in silico guided methods for the rational construction of synthetic promoters and combined them with our targeted fluorescent protein tags. Download the project summary and get an overview of the achievements of our team.</p>
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<a href="#">Download Project Summary</a>
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<div id="mission"> <h3> iGEM Heidelberg Mission 2009: Spybricks </h3>
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<p> Establishing new standards for iGEM, the Heidelberg 2009 team will be concerned with developing ways for measuring promoters in mammalian cells, a default chassis and a first evaluation of the recently postulated BioBrick beta proposal 2 (Tom Knight). Considering the importance of controlling gene expression, our team's work will focus on natural and synthetic mammalian promoters. Our vision is to provide the synthetic biology community with a methodical library of such promoters (with different output strength and sensitivity to different regulatory proteins) and a model which can provide guidance for the development of further synthetic promoters. Our efforts will therefore, from the very beginning, equally entail bioinformatics and wet lab work.</p></div>
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<div id="team"><center><img src="https://static.igem.org/mediawiki/2009/5/50/Team_HD.jpg" alt=""/></center>
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<h3>Team</h3>
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<p>Thirteen students and nine advisors are working on this four month project. We split up into several subgroups whos focus and results you can follow on the Notebook and Results page. If you want to know more about the subgroups and the people involved, meet us on our Team page and let's get to know each other better at the Jamboree in Boston. </p></div>
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<div id="heartbeat"> <center><img src="https://static.igem.org/mediawiki/2009/3/37/Heartbeat_small.gif" alt=""/></center>
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<h3>HEARTBEAT </h3>
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<p>As one of the most important approaches to synthezise synthetic promoters we developed a database that predicts the position of conserved promotor binding sequences. These sequences were identified, analyzed and we coded an easy to use interface that is available for public use. </p></div>
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<div id="notebook"> <center><img src="https://static.igem.org/mediawiki/2009/f/f6/Notebook_HD.jpg" alt=""/></center>
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<h3>Notebook </h3>
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<p>What's about documenation? You will find the entire progress of the project and all the important steps on our Notebook page. The Notebook is divided into the individual subgroups.</p> </div>
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<div id="parts"> <center><img src="https://static.igem.org/mediawiki/2009/c/c0/Parts_HD.jpg" alt=""/></center>
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<h3>Parts </h3>
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<p>Our team submits a library of well characterized and standardized promoters and sensors for eukaryotic cells. We will also contribute the first eucaryotic standart chassis for iGem featuring standardized genome integration sites.</p> </div>
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<div id="gallery"><center><img src="https://static.igem.org/mediawiki/2009/9/93/Notebook.jpg" alt=""/></center>
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<h3>Gallery </h3>
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<p>Spy on our cells or join the Heidelberg Team in the lab with our gallery tour.</p></div>
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<div id="sponsors"> <center><img src="https://static.igem.org/mediawiki/2009/2/29/HD09_sponsors.jpg" alt=""/></center>
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<h3>Sponsors</h3>
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<p>This year we have a lot of distinguished sponsors, which support us and this project. <a href="https://2009.igem.org/Team:Heidelberg/Sponsors">Go here </a> to find out more about them.</p> </div>
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<div id="news">
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<h3>The Team</h3>
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<center><img src="https://static.igem.org/mediawiki/2009/8/89/Team_verySmall.jpg" alt=""/></center>
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<p>This year 13 students started the Heidelberg iGem team.</p>
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<center><embed src="http://www.oneplusyou.com/bb/files/countdown/countdown.swf?co=8fc332&bgcolor=FFFFFF&date_month=11&date_day=09&date_year=0&un=IGEM JAMBOREE 2009&size=normal&mo=10&da=31&yr=2009" type="application/x-shockwave-flash" pluginspage="http://www.macromedia.com/go/getflashplayer" width="240" height="80" wmode="transparent"></embed></center>
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<h3> The iGEM idea </h3>
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<p>iGEM (international genetically engineered machines competition) is an international competition in synthetic biology, hosted by the MIT in Boston. The aim of this competition is to answer a basic question, Randy Rettberg, the director of iGEM once described as follows: "Can simple biological systems be built from standard, interchangeable parts and operated in living cells? Or is biology just too complicated to be engineered in this way?"
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The iGEM-approach to answer that question is to actually try to engineer biological systems with a proper function. Therefore more than 100 interdisciplinary student teams from all over the world, mainly consisting of undergraduate students in biology, biochemistry, engineering, informatics and mathematics, carry out different projects during the summer. These projects reach from medical applications, i.e. genetically modified bacteria used in cancer-treatment to environmental and manufacturing projects, i.e. the construction of a watch-like counter consisting of living cells. In contrast to classical genetic engineering where only one gene is transferred from organism A to organism B, synthetic biology goes forward the construction of whole new systems with a completely new function. Therefore, all iGEM-Teams get access to a gene- Database called registry, where hundreds of different genetic parts with characterized functions are available in a “plug-and-play” –like format. These parts can be simply stuck together to build functional systems.
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The rising number of iGEM-Teams over the last years as well as the upcoming public interest in iGEM, the iGEM-Teams’ projects and synthetic biology in general shows, that synthetic biology will for sure have a great impact in many different fields of both scientific research and every-day life.</p>
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Revision as of 08:18, 13 October 2009

Design your own promoter

As one of the most important approaches to synthezise synthetic promoters we developed a database that predicts the position of conserved promoter binding sequences. We coded an easy to use interface that is available for public use.

Start Design

Mission 2009:
mammalian biobricks

Mammalian synthetic biology has huge potential, but it is in need of new standards and of systematic construction of comprehensive part libraries. Learn more about our new mission on the project page.

Go To Project Page

Mission accomplished

We developed two novel, in silico guided methods for the rational construction of synthetic promoters and combined them with our targeted fluorescent protein tags. Download the project summary and get an overview of the achievements of our team.

Download Project Summary

iGEM Heidelberg Mission 2009: Spybricks

Establishing new standards for iGEM, the Heidelberg 2009 team will be concerned with developing ways for measuring promoters in mammalian cells, a default chassis and a first evaluation of the recently postulated BioBrick beta proposal 2 (Tom Knight). Considering the importance of controlling gene expression, our team's work will focus on natural and synthetic mammalian promoters. Our vision is to provide the synthetic biology community with a methodical library of such promoters (with different output strength and sensitivity to different regulatory proteins) and a model which can provide guidance for the development of further synthetic promoters. Our efforts will therefore, from the very beginning, equally entail bioinformatics and wet lab work.

Team

Thirteen students and nine advisors are working on this four month project. We split up into several subgroups whos focus and results you can follow on the Notebook and Results page. If you want to know more about the subgroups and the people involved, meet us on our Team page and let's get to know each other better at the Jamboree in Boston.

HEARTBEAT

As one of the most important approaches to synthezise synthetic promoters we developed a database that predicts the position of conserved promotor binding sequences. These sequences were identified, analyzed and we coded an easy to use interface that is available for public use.

Notebook

What's about documenation? You will find the entire progress of the project and all the important steps on our Notebook page. The Notebook is divided into the individual subgroups.

Parts

Our team submits a library of well characterized and standardized promoters and sensors for eukaryotic cells. We will also contribute the first eucaryotic standart chassis for iGem featuring standardized genome integration sites.

Sponsors

This year we have a lot of distinguished sponsors, which support us and this project. Go here to find out more about them.

The Team

This year 13 students started the Heidelberg iGem team.

The iGEM idea

iGEM (international genetically engineered machines competition) is an international competition in synthetic biology, hosted by the MIT in Boston. The aim of this competition is to answer a basic question, Randy Rettberg, the director of iGEM once described as follows: "Can simple biological systems be built from standard, interchangeable parts and operated in living cells? Or is biology just too complicated to be engineered in this way?" The iGEM-approach to answer that question is to actually try to engineer biological systems with a proper function. Therefore more than 100 interdisciplinary student teams from all over the world, mainly consisting of undergraduate students in biology, biochemistry, engineering, informatics and mathematics, carry out different projects during the summer. These projects reach from medical applications, i.e. genetically modified bacteria used in cancer-treatment to environmental and manufacturing projects, i.e. the construction of a watch-like counter consisting of living cells. In contrast to classical genetic engineering where only one gene is transferred from organism A to organism B, synthetic biology goes forward the construction of whole new systems with a completely new function. Therefore, all iGEM-Teams get access to a gene- Database called registry, where hundreds of different genetic parts with characterized functions are available in a “plug-and-play” –like format. These parts can be simply stuck together to build functional systems. The rising number of iGEM-Teams over the last years as well as the upcoming public interest in iGEM, the iGEM-Teams’ projects and synthetic biology in general shows, that synthetic biology will for sure have a great impact in many different fields of both scientific research and every-day life.

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