Difference between revisions of "Team:SCU-China/Parts"

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            <h1 class="center">Parts</h1>
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                  <table class="table table-bordered">
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                    <tr>
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                      <th>Number</th>
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                      <th style="text-align: center;">Function</th>
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                    </tr>
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                    <tr>
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                      <td>BBa_K1919000</td>
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                      <td>The CDS of antimicrobial peptide CecropinXJ</td>
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                    </tr>
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                    <tr>
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                      <td>BBa_K1919001</td>
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                      <td>Promotor J23105 + 5-tag system + CDS of CecropinXJ</td>
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                    </tr>
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                    <tr>
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                      <td>BBa_K1919002</td>
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                      <td>Promotor J23106 + 5-tag system + CDS of CecropinXJ</td>
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                    </tr>
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                    <tr>
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                      <td>BBa_K1919003</td>
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                      <td>LacI + LacI Promoter + T7 promotor + 5-tag system + CDS of CecropinXJ</td>
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                    </tr>
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                    <tr>
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                      <td>BBa_K1919100</td>
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                      <td>Induce cell lysis of E.coli when the temperature is raised to 42℃</td>
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                    </tr>
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                    <tr>
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                      <td>BBa_K1919101</td>
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                      <td>Mutant of a temperature-regulated promoter(BBa_K608351) that promote transcription when the temperature is raised up to 37℃, which is more sensitive compared with the wild type.</td>
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                    </tr>
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                    <tr>
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                      <td>BBa_K1919102</td>
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                      <td>Based on part BBa_K1919100 but containing a mutant type of the temperature-regulated promotor so that when at 37℃,this part can kill E.coli at a higher rate.</td>
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                    </tr>
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                    <tr>
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                      <td>BBa_K1919200</td>
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                      <td>AarC expression device. Promoter is J23100</td>
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                    </tr>
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                    <tr>
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                      <td>BBa_K1919204</td>
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                      <td>AarC expression device. Promoter is J23104</td>
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                    </tr>
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                    <tr>
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                      <td>BBa_K1919205</td>
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                      <td>AarC expression device. Promoter is J23105</td>
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                    </tr>
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                    <tr>
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                      <td>BBa_K1919206</td>
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                      <td>AarC expression device. Promoter is J23106</td>
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                    </tr>
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                    <tr>
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                      <td>BBa_K1919212</td>
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                      <td>AarC expression device. Promoter is J23112</td>
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                    </tr>
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                    <tr>
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                      <td>BBa_K1919213</td>
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                      <td>AarC expression device. Promoter is J23113</td>
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                    </tr>
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                    <tr>
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                      <td>BBa_K1919214</td>
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                      <td>AarC expression device. Promoter is J23114</td>
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                    </tr>
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                    <tr>
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                      <td>BBa_K1919233</td>
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                      <td>coding sequence of AarC</td>
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                    </tr>
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                    <tr>
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                      <td>BBa_K1919300</td>
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                      <td>LivJ, a subunit of leucine transportor and is used to increase the absorbation of leucine in liquid LB medium</td>
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                    </tr>
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                    <tr>
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                      <td>BBa_K1919301</td>
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                      <td>LivF, a subunit of leucine transportor and is used to increase the absorbation of leucine in liquid LB medium</td>
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                    </tr>
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                    <tr>
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                      <td>BBa_K1919302</td>
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                      <td>LivG, a subunit of leucine transportor and is used to increase the absorbation of leucine in liquid LB medium</td>
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                    </tr>
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                    <tr>
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                      <td>BBa_K1919303</td>
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                      <td>LivH, a subunit of leucine transportor and is used to increase the absorbation of leucine in liquid LB medium</td>
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                    </tr>
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                    <tr>
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                      <td>BBa_K1919304</td>
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                      <td>LivK, a subunit of leucine transportor and is used to increase the absorbation of leucine in liquid LB medium</td>
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                    </tr>
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                    <tr>
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                      <td>BBa_K1919305</td>
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                      <td>LivM, a subunit of leucine transportor and is used to increase the absorbation of leucine in liquid LB medium</td>
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                    </tr>
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                    <tr>
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                      <td>BBa_K1919400</td>
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                      <td>Homologous substitution fragment for RED recombination, containing a chloramphenicol-resistant gene with a homology arm on each side. For replacing the tryptophanase gene in E. coli.</td>
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                    </tr>
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                    <tr>
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                      <td>BBa_K1919500</td>
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                      <td>For the measurement of characters of VHb gene(K1321200) in E.coli</td>
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                    </tr>
  
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<p>Each team will make new parts during iGEM and will submit them to the Registry of Standard Biological Parts. The iGEM software provides an easy way to present the parts your team has created. The <code>&lt;groupparts&gt;</code> tag (see below) will generate a table with all of the parts that your team adds to your team sandbox.</p>
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<p>Remember that the goal of proper part documentation is to describe and define a part, so that it can be used without needing to refer to the primary literature. Registry users in future years should be able to read your documentation and be able to use the part successfully. Also, you should provide proper references to acknowledge previous authors and to provide for users who wish to know more.</p>
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<h5>Note</h5>
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<p>Note that parts must be documented on the <a href="http://parts.igem.org/Main_Page"> Registry</a>. This page serves to <i>showcase</i> the parts you have made. Future teams and other users and are much more likely to find parts by looking in the Registry than by looking at your team wiki.</p>
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<h5>Adding parts to the registry</h5>
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<p>You can add parts to the Registry at our <a href="http://parts.igem.org/Add_a_Part_to_the_Registry">Add a Part to the Registry</a> link.</p>
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<p>We encourage teams to start completing documentation for their parts on the Registry as soon as you have it available. The sooner you put up your parts, the better you will remember all the details about your parts. Remember, you don't need to send us the DNA sample before you create an entry for a part on the Registry. (However, you <b>do</b> need to send us the DNA sample before the Jamboree. If you don't send us a DNA sample of a part, that part will not be eligible for awards and medal criteria.)</p>
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<h5>What information do I need to start putting my parts on the Registry?</h5>
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<p>The information needed to initially create a part on the Registry is:</p>
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<li>Part Name</li>
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<li>Part type</li>
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<li>Creator</li>
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<li>Sequence</li>
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<li>Short Description (60 characters on what the DNA does)</li>
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<li>Long Description (Longer description of what the DNA does)</li>
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<li>Design considerations</li>
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We encourage you to put up <em>much more</em> information as you gather it over the summer. If you have images, plots, characterization data and other information, please also put it up on the part page. </p>
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<h5>Inspiration</h5>
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<p>We have a created  a <a href="http://parts.igem.org/Well_Documented_Parts">collection of well documented parts</a> that can help you get started.</p>
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<p> You can also take a look at how other teams have documented their parts in their wiki:</p>
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<li><a href="https://2014.igem.org/Team:MIT/Parts"> 2014 MIT </a></li>
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<li><a href="https://2014.igem.org/Team:Heidelberg/Parts"> 2014 Heidelberg</a></li>
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<li><a href="https://2014.igem.org/Team:Tokyo_Tech/Parts">2014 Tokyo Tech</a></li>
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<h5>Part Table </h5>
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<groupparts>iGEM2016 Example</groupparts>
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Latest revision as of 12:06, 28 November 2016

Parts

Number Function
BBa_K1919000 The CDS of antimicrobial peptide CecropinXJ
BBa_K1919001 Promotor J23105 + 5-tag system + CDS of CecropinXJ
BBa_K1919002 Promotor J23106 + 5-tag system + CDS of CecropinXJ
BBa_K1919003 LacI + LacI Promoter + T7 promotor + 5-tag system + CDS of CecropinXJ
BBa_K1919100 Induce cell lysis of E.coli when the temperature is raised to 42℃
BBa_K1919101 Mutant of a temperature-regulated promoter(BBa_K608351) that promote transcription when the temperature is raised up to 37℃, which is more sensitive compared with the wild type.
BBa_K1919102 Based on part BBa_K1919100 but containing a mutant type of the temperature-regulated promotor so that when at 37℃,this part can kill E.coli at a higher rate.
BBa_K1919200 AarC expression device. Promoter is J23100
BBa_K1919204 AarC expression device. Promoter is J23104
BBa_K1919205 AarC expression device. Promoter is J23105
BBa_K1919206 AarC expression device. Promoter is J23106
BBa_K1919212 AarC expression device. Promoter is J23112
BBa_K1919213 AarC expression device. Promoter is J23113
BBa_K1919214 AarC expression device. Promoter is J23114
BBa_K1919233 coding sequence of AarC
BBa_K1919300 LivJ, a subunit of leucine transportor and is used to increase the absorbation of leucine in liquid LB medium
BBa_K1919301 LivF, a subunit of leucine transportor and is used to increase the absorbation of leucine in liquid LB medium
BBa_K1919302 LivG, a subunit of leucine transportor and is used to increase the absorbation of leucine in liquid LB medium
BBa_K1919303 LivH, a subunit of leucine transportor and is used to increase the absorbation of leucine in liquid LB medium
BBa_K1919304 LivK, a subunit of leucine transportor and is used to increase the absorbation of leucine in liquid LB medium
BBa_K1919305 LivM, a subunit of leucine transportor and is used to increase the absorbation of leucine in liquid LB medium
BBa_K1919400 Homologous substitution fragment for RED recombination, containing a chloramphenicol-resistant gene with a homology arm on each side. For replacing the tryptophanase gene in E. coli.
BBa_K1919500 For the measurement of characters of VHb gene(K1321200) in E.coli