Difference between revisions of "Team:NAIT Edmonton/Trial11"

 
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<title>Team NAIT 2015</title>
 
<title>Team NAIT 2015</title>
 
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</div>
 
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</div>
 
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  <div id="wrap">
 
 
<div id="accordion">
 
  <h3>Section 1</h3>
 
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    Mauris mauris ante, blandit et, ultrices a, suscipit eget, quam. Integer
 
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  <h3>Section 2</h3>
 
  <div>
 
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    Sed non urna. Donec et ante. Phasellus eu ligula. Vestibulum sit amet
 
    purus. Vivamus hendrerit, dolor at aliquet laoreet, mauris turpis porttitor
 
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  <h3>Section 3</h3>
 
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    Phasellus pellentesque purus in massa. Aenean in pede. Phasellus ac libero
 
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    <ul>
 
      <li>List item one</li>
 
      <li>List item two</li>
 
      <li>List item three</li>
 
    </ul>
 
  </div>
 
  <h3>Section 4</h3>
 
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    <p>
 
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<center><div class="top_slogan">The Project</div></center>
 
  
<h1>Background</h1></a>
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<p style="font-size:15px">The structural and functional study of the proteins expressed by a genome is
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called proteomics. This relatively novel science uses different methodologies in order to
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separate and identify specific proteins of interest. Among these techniques, SDS-PAGE
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plays an essential role due to its high sensitivity, low sample volume requirement, and
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high popularity. Negatively charged proteins migrate towards the positive electrode
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according to their size and charge. Smaller proteins migrate further in a given amount of
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time. As proteins are separated in this manner, users load molecular weight standards
+
<div class="flexslider">
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    <ul class="slides">
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    <li><a href=""><img src="https://static.igem.org/mediawiki/2015/6/62/NAIT_Slide_Pedway.jpg" alt="" title="" border="0"/></a>
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            <div class="flex-caption">
 +
                <h2></h2>
 +
                    <p><strong><a href=""></a></strong></p>
 +
                </div>
 +
            </li>
 +
            <li><a href="https://2015.igem.org/Team:NAIT_Edmonton/Desc"><img src="https://static.igem.org/mediawiki/2015/5/56/NAIT_Slide_1_Project.jpg"alt="" title="" border="0"/></a>
 +
            <div class="flex-caption">
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                <h2></h2>
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                    <p></p>
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                </div>
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            </li>
 +
            <li><a href="https://2015.igem.org/Team:NAIT_Edmonton/Practices"><img src="https://static.igem.org/mediawiki/2015/d/db/NAIT_Slide_2_Whiteboard.jpg" alt="" title="" border="0"/></a>
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            <div class="flex-caption">
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                <h2></h2>
 +
                   
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                    <p></p>
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                </div>
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            </li>
 +
            <li><a href="https://2015.igem.org/Team:NAIT_Edmonton/Modeling"><img src="https://static.igem.org/mediawiki/2015/5/57/NAIT_Slide_3_3D.jpg"alt="" title="" border="0"/></a>
 +
            <div class="flex-caption">
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                <h2></h2>
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                    <p></p>
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                </div>
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            </li>
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    </ul>
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to estimate the size (in kDa) of the proteins present in their sample. Once the proteins of
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<div id="wrap5">
  
a single sample have been isolated and are embedded in the polyacrylamide (PA) gel
+
  <div class="section_one_three">
 +
        <h2 class="centered_title">Achievements</h2>
 +
        <div class="roundimg"><a href="https://2015.igem.org/Team:NAIT_Edmonton/Achievements" title=""><img src="https://static.igem.org/mediawiki/2015/5/50/NAIT_Medal_Icon.png" width="125px" alt="" title="" /></a></div>
 +
        <p class="centered_text">
 +
Despite the time constraints, our team achieved a lot this summer and we are proud of what we have accomplished.
 +
        </p>
 +
        <a href="https://2015.igem.org/Team:NAIT_Edmonton/Achievements" class="more">read more</a>
 +
        </div>
 +
       
 +
  <div class="section_one_three">
 +
        <h2 class="centered_title">iGEM 2015</h2>
 +
        <div class="roundimg"><a href="https://2015.igem.org" title=""><img src="https://static.igem.org/mediawiki/2015/0/05/NAIT_Icon_services.png" alt="" title="" /></a></div>
 +
        <p class="centered_text">
 +
Learn about the exciting opportunities the iGEM foundation has to offer! The experience was incredible!
 +
        </p>
 +
        <a href="https://2015.igem.org" class="more">read more</a>
 +
        </div>
  
matrix, staining procedures are used to visualize them.</p>
+
  <div class="section_one_three">
 +
        <h2 class="centered_title">Contact Us!</h2>
 +
        <div class="roundimg"><a href="https://2015.igem.org/Team:NAIT_Edmonton/ContactUs" title=""><img src="https://static.igem.org/mediawiki/2015/2/29/NAIT_Icon_contact.png" alt="" title="" /></a></div>
 +
        <p class="centered_text">
 +
Please contact our team if you want more information about our project or have any other questions or concerns.
 +
        </p>
 +
        <a href="https://2015.igem.org/Team:NAIT_Edmonton/ContactUs" class="more">read more</a>
 +
        </div>
 +
 
 +
</div>  
  
<br>
 
  
<center><img src="http://upload.wikimedia.org/wikipedia/commons/4/46/SDS-PAGE_Electrophoresis.png" width="750px"></center>
+
  <div class="clear"></div>  
 +
 
 +
 
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</div>
  
<br>
 
  
<p style="font-size:15;">Organic dyes, such as Coomassie blue, can be used for this purpose;
 
 
nevertheless, their low sensitivity and a detection range that goes from 1 to 50 ng can
 
 
be a challenge for detecting low abundance proteins (Jin, Huang, Yoo, & Choi, 2006). A
 
 
higher sensitivity can be achieved by fluorescent staining techniques (from 0.1 to 10
 
 
ng.); however, UV instruments are necessary in order to read the data (Jin et al., 2006).
 
 
The most sensitive method up to date is radiolabeling, but the requirement of hazardous
 
 
isotopes and their complex management makes it a complicated procedure (Jin et al.,
 
 
2006). Silver staining is a method that offers great sensitivity and an easy to handle
 
 
protocol, thus making it one of the most commonly used staining methods. </p>
 
 
<br>
 
 
<center><img src="http://www.bio-rad.com/webroot/web/images/lsr/products/electrophoresis/product_overlay_content/global/lsr_biosafe_coomasie_gel.jpg"></center>
 
 
<br><br>
 
 
<h1>The Problem </h1></a>
 
 
<p style="font-size:15px">Difficulties with silver staining arise when the molecular weight markers are re-
 
 
colored golden-brown in the staining process. Markers offer evenly distributed proteins
 
 
that show bands of equal intensity and known size. Researchers can compare these
 
 
bands with their sample and identify the protein they are looking for based on its size. A
 
 
subset of these markers has color-coded standard proteins to facilitate the identification
 
 
of each band. Post-silver staining, the users lose the ability to use the color code as a
 
 
reference.</p>
 
 
<br>
 
 
<center><img src="http://labs.mmg.pitt.edu/gjoerup/silver_stain.jpg" width="750px"></center>
 
     
 
  </div>
 
  </div>
 
 
  <div class="clear"></div>
 
  
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<!----------
 
 
                          _ __  _
 
                        ;'  '',)
 
                        /;6 , ;/
 
                        (Y)_:., |
 
                        `-', :; \
 
                          |;  ,.:\
 
                          /:.;  ;;)
 
                        |:;,.'|  :/
 
                        / |:  / ; /
 
                      /:;\ `| "//
 
                      /_,: | |./,|
 
                    _/: \.'|,|/| |
 
                  /:.,:.|,|"| |:|
 
                  /:;:|:,/;|:| |'|
 
        eduardo  |',:| \_ \ |_|;\_
 
                /;\_ /\_)) \_))\_))
 
                (;(________
 
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Latest revision as of 20:44, 6 August 2015

Team NAIT 2015