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- | {{MIT-header2}}
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- | {{MIT-style-team}}
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- | <html>
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- | <head>
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- | <link href="http://ajax.googleapis.com/ajax/libs/jqueryui/1.8/themes/base/jquery-ui.css" rel="stylesheet" type="text/css"/>
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- | <script src="http://ajax.googleapis.com/ajax/libs/jquery/1.5/jquery.min.js"></script>
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- | <script src="http://ajax.googleapis.com/ajax/libs/jqueryui/1.8/jquery-ui.min.js"></script>
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- | | + | |
- | | + | |
- | <!-- TODO: add pre/n buttons -->
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- | <script>
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- | $(document).ready(function(){ | + | |
- | $('.bio').css('display','none');
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- | $('.col_list li').css('cursor','pointer');
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- | $('.col_list li').hover(function() {
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- | $(this).css('background-color','#a3abae');
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- | }, function() {
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- | $(this).css('background-color','#ffffff');
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- | });
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- | $("#accordion").accordion();
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- | $('.col_list li').click(function () {
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- | $('.bio').hide();
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- | var name = $(this).attr('id');
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- | $('#'+name+'bio').fadeIn(500);
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- | });
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- | });
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- | </script>
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- | </head>
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- | <body>
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- | <div id="col_nav">
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- | <div id="accordion">
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- | <h3><a href="#">Overview</a></h3>
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- | <div class="col_list">
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- | <ul>
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- | <li id="aa1">Placeholder</li>
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- | </ul>
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- | </div><!-- end overview -->
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- | <h3><a href="#">Biobricks</a></h3>
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- | <div class="col_list">
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- | <ul>
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- | <li id="a1">Placeholder</li>
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- | </ul>
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- | </div><!-- end biobricks -->
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- | | + | |
- | <h3><a href="#">Foundational</a></h3>
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- | <div class="col_list">
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- | <ul>
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- | <li id="b1">In Vitro </li>
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- | <li id="b2">Nucleic Acid Delivery</li>
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- | <li id="b3">In Vivo Strand Displacement </li>
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- | </ul>
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- | </div><!-- end foundational -->
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- | | + | |
- | <h3><a href="#">Sensing</a></h3>
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- |
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- | <div class="col_list">
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- | <ul>
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- | <li id="iv1">Modeling</li>
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- | <li id="iv2">In Vitro Sensing</li>
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- | </ul>
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- | </div><!-- end sensing-->
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- | | + | |
- | <h3><a href="#">Processing</a></h3>
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- |
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- | <div class="col_list">
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- | <ul>
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- | <li id="m1"> Modeling </li>
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- | <li id="m2"> In Vitro Not Gate </li>
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- | <li id="m3"> Hammerhead Ribozymes </li>
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- | </ul>
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- | </div><!-- end processing-->
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- | <h3><a href="#">Actuation</a></h3>
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- | <div class="col_list">
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- | <ul>
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- | <li id="m4"> Modeling </li>
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- | <li id="m5"> In Vitro </li>
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- | <li id="m6"> In Vivo </li>
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- | </ul>
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- | </div><!-- end actuation-->
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- | </div>
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- | </div><!--end col_nav-->
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- | <div id="col_left">
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- | <div class="bio" id="b1bio">
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- | <b> [RNA Strand Displacement In Vitro] </b>
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- | <br>
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- | <br>
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- | <br> Our team first decided to repeat the results of Winfree / Qian's 2011 paper on strand displacement, but using 2'-O-Methyl RNA tagged with fluorophores and quenchers.
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- | <br>
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- | <b> Figure A </b>
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- | <img src="https://static.igem.org/mediawiki/2012/e/ea/Foundation1MIT.png"/>
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- | </div>
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- | <div class="bio" id="b2bio">
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- | <b> Nucleic Acid Delivery </b>
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- | <br>
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- | <br>
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- | <br>
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- | <b> Delivery of Plasmid DNA to Mammalian Cells </b>
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- | <br>
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- | <br>
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- | <br> Constitutive Expression of fluorescent markers etc
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- | <br>
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- | <b> Delivery of 2'-O-Me RNA to Mammalian Cells </b>
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- | <br>
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- | <br> Movie of HEK293 cell being transfected with T*-S6*-ROX, as well as static images
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- | <br> 15,20,25,30 pmol ratio data from FACS
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- | <br>
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- | <br>
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- | <b> Inducible Control of Protein Expression </b>
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- | <br>
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- | <br> DOX curve
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- | <br>
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- | <br>
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- | <b> Delivery of Plasmid DNA which transcribes short RNA Inputs </b>
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- | <br>
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- | <br> FF1 Knockdown Data
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- | </div>
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- | <div class="bio" id="b3bio">
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- | <b>In Vivo RNA Strand Displacement </b>
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- | <br>
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- | <br>
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- | <b> Strategy 1: Lipofectamine 2000 Transfection of RNA version of Reporter from Winfree/QIan 2011 Paper</b>
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- | <br>
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- | <br>
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- | <br> Images will go here from April 24th experiment - display red fluorescence in all wells, including those that only got reporter or the wrong input - also see red vesicles indicating reporter comes apart inside the vesicles
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- | <br>
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- | <br>
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- | <br> Strategy 2: Switch Transfection reagent to RNAiMAX </b>
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- | <br>
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- | <br> RNAiMAX is supposed to be a better transfection reagent for double stranded RNA
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- | <br>
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- | <br> Images will go here from experiment from June 13th onward where we do not see red vesicles, however we still see whole cell red fluorescence
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- | <br>
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- | <br>
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- | <b> Strategy 3: Tag RNA strand with an Alexa Fluorophore to act as a transfection marker </b>
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- | <br>
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- | <br>
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- | <b> Strategy 4: Create DNA plasmids driving transcription of RNA inputs, while transfecting RNA Reporter </b>
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- | <br>
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- | <br>
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- | <b> Strategy 4: Nucleofect RNA reporter, RNA inputs </b>
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- | <br>
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- | <br>
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- | <b> [Strategy 5]: Redesign RNA Reporter </b>
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- | </div>
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- | <div id='next' style="float:right; margin-top: 20px;"> </div>
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- | </div><!--end col_left-->
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- | </body>
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- | </html>
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DEPRECATED. DO NOT EDIT.