Difference between revisions of "Team:HSNU-TAIPEI/Part Collection"

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      <h1>Part Collection</h1>
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      <div class="section">
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        <article class="article">
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          <h3 class="article-title">AFB1</h3>
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            <ul class="article-ul">
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                <li><a href="http://parts.igem.org/Part:BBa_K1613000">BBa_K1613000</a><span>J22106+B0032</span></li>
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                <li><a href="http://parts.igem.org/Part:BBa_K1613001">BBa_K1613001</a><span>J23119+B0032</span></li>
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                <li><a href="http://parts.igem.org/Part:BBa_K1613002">BBa_K1613002</a><span>J22106+B0034</span></li>
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                <li><a href="http://parts.igem.org/Part:BBa_K1613003">BBa_K1613003</a><span>CYP1A2+B0015</span></li>
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                <li><a href="http://parts.igem.org/Part:BBa_K1613004">BBa_K1613004</a><span>CYP1A2</span><span><mark>(Basic Part)</mark></span></li>
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                <li><a href="http://parts.igem.org/Part:BBa_K1613005">BBa_K1613005</a><span>J23119+B0030+CYP1A2+B0015</span></li>
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                <li><a href="http://parts.igem.org/Part:BBa_K1613006">BBa_K1613006</a><span>J23119+B0032+CYP1A2+B0015</span></li>
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<h4 class="article-h4"> &#10004; A composite part that can detect some toxins.</h4>
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<p class="article-p">cyp1a2 can oxidize the substances that it can metabolism. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. CYP1A2 is able to metabolize some PAHs to carcinogenic intermediates. Other xenobiotic substrates for this enzyme include aflatoxin B1, and acetaminophen.</p>
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<img src="">
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<li><a href="http://parts.igem.org/Part:BBa_K1613007">BBa_K1613007</a><span>J23119+B0034+CYP1A2+B0015</span></li>
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<h4 class="article-h4"> &#10004; A composite part that can detect some toxins.</h4>
 +
<p class="article-p">cyp1a2 can oxidize the substances that it can metabolism. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. CYP1A2 is able to metabolize some PAHs to carcinogenic intermediates. Other xenobiotic substrates for this enzyme include aflatoxin B1, and acetaminophen.</p>
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<img src="">
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                <li><a href="http://parts.igem.org/Part:BBa_K1613008">BBa_K1613008</a><span>J22106+B0032+E0040+B0015</span></li>
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                <li><a href="http://parts.igem.org/Part:BBa_K1613009">BBa_K1613009</a><span>J22106+B0032+E1010+B0015</span></li>
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                <li><a href="http://parts.igem.org/Part:BBa_K1613010">BBa_K1613010</a><span>J22106+B0034+E0040+B0015</span></li>
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                <li><a href="http://parts.igem.org/Part:BBa_K1613011">BBa_K1613011</a><span>J22106+B0034+E1010+B0015</span></li>
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            </ul>
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        </article>
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        <article class="article">
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          <h3 class="article-title">Benzo[a]pyrene</h3>
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            <ul class="article-ul">
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              <li><a href="http://parts.igem.org/Part:BBa_K1613012">BBa_K1613012</a><span>J23113+B0034+K1092104+B0034+K1092000+B0015</span></li>
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<h4 class="article-h4"> &#10004; QsrR Binding Site inhibits the transcription and translation of Red Fluorescent Protein.</h4>
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<p class="article-p">There is a QsrR Binding Site between promoter and RBS. Which can combine with Quinone-sensing and response Repressor(QsrR). And inhibit the transcription. While QsrR combines with BaP-1,6-Quinone, the QsrR will be activated and depart the Binding Site. That makes the transcription of downstream.</p>
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<img src="">
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<li><a href="http://parts.igem.org/Part:BBa_K1613013">BBa_K1613013</a><span>J23113+B0034+E1010+B0015</span></li>
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              <li><a href="http://parts.igem.org/Part:BBa_K1613020">BBa_K1613020</a><span></span></li>
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            </ul>
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        </article>
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        <article class="article">
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          <h3 class="article-title">Cadmium</h3>
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            <ul class="article-ul">
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            <li><a href="http://parts.igem.org/Part:BBa_K1613016">BBa_K1613016</a><span>K896008+B0032</span></li>
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<h4 class="article-h4"> &#10004; is a new part which can detect cadmium in ions in the liquid.</h4>
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<p class="article-p">This part is designed to proceed cadmium detection in e.coli.Zintp K896008 is a promoter which is designed by NYMU in 2013.It is a part highly specific to the cadmium.The promoter can trigger the RFP. We combine these part to detect cadmium.</p>
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<img src="">
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</ul>
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        </article>
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        <article class="article">
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          <h3 class="article-title">Lead</h3>
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            <ul class="article-ul">
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              <li><a href="http://parts.igem.org/Part:BBa_K1613017">BBa_K1613017</a><span></span></li>
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<h4 class="article-h4"> &#10004; K1613017 is a new part which can detect lead (Pb) ions in the liquid.</h4>
 +
<p class="article-p">This part is desinged to proceed lead detection in e.coli. When lead ions (Pb<sup>2+</sup>) enter the e.coli, they will combine with the protein PbrR and then form a dimer. The lead promoter can be controlled by the dimer to further trigger the RFP. The idea of this design came from Brown 2007 igem team, also working on lead detection. We combined I721001 and I721002 from their teams with a constitutive promoter J23102 and RFP to make them function.</p>
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<img src="">
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</ul>
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        </article>
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              </div>
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</div>
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</main>
  
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<h2> Part Collection</h2>
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        <img src="https://static.igem.org/mediawiki/2015/f/f8/HSNU-TAIPEI_cooperation_1.gif">
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<h4>Note</h4>
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        <img src="https://static.igem.org/mediawiki/2015/3/37/HSNU-TAIPEI_cooperation_2.png">
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<p>In order to be considered for the <a href="https://2015.igem.org/Judging/Awards#SpecialPrizes">Best Part Collection award</a>, you must fill out this page.</p>
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        <img src="https://static.igem.org/mediawiki/2015/0/02/HSNU-TAIPEI_cooperation_3.png">
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        <img src="https://static.igem.org/mediawiki/2015/9/92/HSNU-TAIPEI_cooperation_4.png">
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        <img src="https://static.igem.org/mediawiki/2015/e/e8/HSNU-TAIPEI_cooperation_5.png">
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        <img src="https://static.igem.org/mediawiki/2015/6/60/HSNU-TAIPEI_cooperation_6.png">
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        <img src="https://static.igem.org/mediawiki/2015/9/9a/HSNU-TAIPEI_attributions_1.gif">
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</div>
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<p><a href="http://www.hs.ntnu.edu.tw">HSNU | Taipei</a></p>
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</footer>
 
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<p>Did your team make a lot of great parts? Is there a theme that ties all your parts together? Do you have more than 10 parts in this collection? Did you make a CRISPR collection, a MoClo collection, or a collection of awesome pigment parts? Describe your parts collection on this page, so the judges can evaluate you for the Best Part Collection award.</p>
 
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{{HSNU-TAIPEI/nav_js}}

Latest revision as of 07:48, 26 November 2015

Part Collection

AFB1

  • BBa_K1613000J22106+B0032
  • BBa_K1613001J23119+B0032
  • BBa_K1613002J22106+B0034
  • BBa_K1613003CYP1A2+B0015
  • BBa_K1613004CYP1A2(Basic Part)
  • BBa_K1613005J23119+B0030+CYP1A2+B0015
  • BBa_K1613006J23119+B0032+CYP1A2+B0015

    • ✔ A composite part that can detect some toxins.

    cyp1a2 can oxidize the substances that it can metabolism. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. CYP1A2 is able to metabolize some PAHs to carcinogenic intermediates. Other xenobiotic substrates for this enzyme include aflatoxin B1, and acetaminophen.

  • BBa_K1613007J23119+B0034+CYP1A2+B0015

    • ✔ A composite part that can detect some toxins.

    cyp1a2 can oxidize the substances that it can metabolism. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. CYP1A2 is able to metabolize some PAHs to carcinogenic intermediates. Other xenobiotic substrates for this enzyme include aflatoxin B1, and acetaminophen.

  • BBa_K1613008J22106+B0032+E0040+B0015
  • BBa_K1613009J22106+B0032+E1010+B0015
  • BBa_K1613010J22106+B0034+E0040+B0015
  • BBa_K1613011J22106+B0034+E1010+B0015

Benzo[a]pyrene

  • BBa_K1613012J23113+B0034+K1092104+B0034+K1092000+B0015

    • ✔ QsrR Binding Site inhibits the transcription and translation of Red Fluorescent Protein.

    There is a QsrR Binding Site between promoter and RBS. Which can combine with Quinone-sensing and response Repressor(QsrR). And inhibit the transcription. While QsrR combines with BaP-1,6-Quinone, the QsrR will be activated and depart the Binding Site. That makes the transcription of downstream.

  • BBa_K1613013J23113+B0034+E1010+B0015
  • BBa_K1613020

Cadmium

  • BBa_K1613016K896008+B0032

    • ✔ is a new part which can detect cadmium in ions in the liquid.

    This part is designed to proceed cadmium detection in e.coli.Zintp K896008 is a promoter which is designed by NYMU in 2013.It is a part highly specific to the cadmium.The promoter can trigger the RFP. We combine these part to detect cadmium.

Lead

  • BBa_K1613017

    • ✔ K1613017 is a new part which can detect lead (Pb) ions in the liquid.

    This part is desinged to proceed lead detection in e.coli. When lead ions (Pb2+) enter the e.coli, they will combine with the protein PbrR and then form a dimer. The lead promoter can be controlled by the dimer to further trigger the RFP. The idea of this design came from Brown 2007 igem team, also working on lead detection. We combined I721001 and I721002 from their teams with a constitutive promoter J23102 and RFP to make them function.