Team:LZU-China/Project

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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 <a href="https://2008.igem.org/Help:Template/Examples">HERE</a>.
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{| style="color:#1b2c8a;background-color:#0c6;" cellpadding="3" cellspacing="1" border="1" bordercolor="#fff" width="62%" align="center"
 
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!align="center"|[[Team:LZU-China|Home]]
 
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!align="center"|[[Team:LZU-China/Team|Team]]
 
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!align="center"|[https://igem.org/Team.cgi?year=2013&team_name=LZU-China Official Team Profile]
 
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!align="center"|[[Team:LZU-China/Project|Project]]
 
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!align="center"|[[Team:LZU-China/Parts|Parts Submitted to the Registry]]
 
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!align="center"|[[Team:LZU-China/Modeling|Modeling]]
 
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!align="center"|[[Team:LZU-China/Notebook|Notebook]]
 
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!align="center"|[[Team:LZU-China/Safety|Safety]]
 
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!align="center"|[[Team:LZU-China/Attributions|Attributions]]
 
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|}
 
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== '''Overall project''' ==
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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)
 
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== Project Details==
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<title>progect</title>
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<body>
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=== Part 2 ===
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<div class="body-in">
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    <div class="main-top">
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        <div class="logo">
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        <div class="op-box">
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            <a target="_self" href="https://2013.igem.org/wiki/index.php?title=Team:LZU-China/Project&action=edit">edit</a>
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            <a target="_self" href="https://2013.igem.org/Team:LZU-China/Team">view</a>
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            </div>
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        </div>
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        <ul class="main-items">
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            <a href="https://2013.igem.org/Team:LZU-China"><li class="item1">Home</li></a>
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            <a href="https://2013.igem.org/Team:LZU-China/Team"><li>Team</li></a>
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            <a href="https://igem.org/Team.cgi?year=2013&team_name=LZU-China"><li>Profile</li></a>
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            <a href="https://2013.igem.org/Team:LZU-China/Project"><li class="selected">Project</li></a>
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            <a href="https://2013.igem.org/Team:LZU-China/Parts"><li>Parts</li></a>
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            <a href="https://2013.igem.org/Team:LZU-China/Notebook"><li>Notebook</li></a>
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            <a href="https://2013.igem.org/Team:LZU-China/Safety"><li>Safety</li></a>
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            <a href="https://2013.igem.org/Team:LZU-China/Attributions"><li>Attributions</li></a>
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            <a href="https://2013.igem.org/Team:LZU-China/HumanPractice"><li>H.P.</li></a>
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    </div>
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    <div class="main-center" id="main-center">
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        <div class="center-left" id="center-left">
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        <a href="#h-Design & Device"><h1>Design & Device</h1></a>
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        <a href="#h-Expriments"><h1>Expriments</h1></a>
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        </div>
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        <div class="center-right">
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<h2> <span class="mw-headline" id="h-Design & Device">Design & Device</span></h2>
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<h3> <span class="mw-headline" id="Promoter">Promoter: 4 copies of NFκB gene </span></h3>
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On the basis of NF-κB signaling pathway and its feedback loop dynamics, we provided a device: A high-throughput drug screening system. The system is used to screen targeted drugs in NF-κB signaling pathway and lasts even longer. Natrually, we could  estimate whether the kind of drug is good or not.
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<br><img src="https://static.igem.org/mediawiki/2013/6/64/LZU-China_Project_1.png"/>
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<br><br>NF-κB is a DNA binding protein, which means that the dimer could recognize a certain gene sequence and bind with it. Thus, we designed a four coupies of NF-κB gene sequence as the promoter. The downstream gene IκB flag with GFP, which could be a controller in tumor invading,moreover , easy to observe.
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</p>
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=== The Experiments ===
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<h2> <span class="mw-headline" id="h-Expriments">Expriments</span></h2>
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4X-NFκB-IκBα-4.20 was tranfected in DU145 cells, Hep-G2, Changliver cells. Since the these kinds of cells have background expression of NF-κB, we use gene knockout technology to remove these parts of gene.
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These images were taken with a cooled CCD camera 1 day after transfection using the fluorescent microscope. The images all showed that our promoter 4X-NFκB responsed in a good condition by that time, and the difference of brightness of the fluorescent also provide a evidence that our recombainat vector works well.
 +
Additionally, we will do some experiments to transfect  DU145, 293T and Hela cells with the vector for establishment of stable cell lines for further research.
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<br><img src="https://static.igem.org/mediawiki/2013/f/f7/Initpintu_LZU.jpg"/>
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        </div>
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    </div>
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    <div class="main-bottom">
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    LanZhou University | 222 TianShui South Road, ChengGuan District, LanZhou, China, 730000<br>
 +
        E-mail:hwang2013@lzu.edu.cn<br>
 +
LanZhou University © 2013 <a target="_new" href="http://en.lzu.edu.cn">Privacy Policy</a>
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Latest revision as of 04:01, 28 September 2013

progect

Design & Device

Promoter: 4 copies of NFκB gene

On the basis of NF-κB signaling pathway and its feedback loop dynamics, we provided a device: A high-throughput drug screening system. The system is used to screen targeted drugs in NF-κB signaling pathway and lasts even longer. Natrually, we could estimate whether the kind of drug is good or not.


NF-κB is a DNA binding protein, which means that the dimer could recognize a certain gene sequence and bind with it. Thus, we designed a four coupies of NF-κB gene sequence as the promoter. The downstream gene IκB flag with GFP, which could be a controller in tumor invading,moreover , easy to observe.

Expriments

4X-NFκB-IκBα-4.20 was tranfected in DU145 cells, Hep-G2, Changliver cells. Since the these kinds of cells have background expression of NF-κB, we use gene knockout technology to remove these parts of gene. These images were taken with a cooled CCD camera 1 day after transfection using the fluorescent microscope. The images all showed that our promoter 4X-NFκB responsed in a good condition by that time, and the difference of brightness of the fluorescent also provide a evidence that our recombainat vector works well. Additionally, we will do some experiments to transfect DU145, 293T and Hela cells with the vector for establishment of stable cell lines for further research.
LanZhou University | 222 TianShui South Road, ChengGuan District, LanZhou, China, 730000
E-mail:hwang2013@lzu.edu.cn
LanZhou University © 2013 Privacy Policy