Difference between revisions of "Team:Jilin China/Parts"

 
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   <section class="s2">
 
   <section class="s2">
 
   <ul>
 
   <ul>
    <li class="toBeDeletedAlert full-width" id="">
 
    <div>
 
      <h2>Editing Alert!</h2>
 
  
      <h3>Note</h3>
 
      <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>
 
      <p>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>
 
      <p>Please include a table of all the parts your team has made during your project on this page. Remember part characterization and measurement data must go on your team part pages on the Registry. </p>
 
 
      <h3>What information do I need to start putting my parts on the Registry?</h3>
 
      <p>The information needed to initially create a part on the Registry is:</p>
 
 
      <h3>Inspiration</h3>
 
      <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>
 
      <ul>
 
            <li>Part Name</li>
 
            <li>Part type</li>
 
            <li>Creator</li>
 
            <li>Sequence</li>
 
            <li>Short Description (60 characters on what the DNA does)</li>
 
            <li>Long Description (Longer description of what the DNA does)</li>
 
            <li>Design considerations</li>
 
      </ul>
 
    </div>
 
    </li>
 
 
     <li class="paragraph_1 start" id="paragraph_1">
 
     <li class="paragraph_1 start" id="paragraph_1">
 
     <div>
 
     <div>
 
       <h2>Introduction</h2>
 
       <h2>Introduction</h2>
         <p>This year, we build hundreds of parts, including xxx basic parts and xxx composite parts. You can see more details in the part registry page. </p>
+
         <p>This year, Jilin_China build hundreds of parts, including 90 basic parts, 7 composite parts and 3 part collections. If you want to see more details, you can find the usage and characterization in the part registry page. You can also visit the basic part, composite part and part collection page for more information.</p>
 
     </div>
 
     </div>
 
     </li>
 
     </li>
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     <div>
 
     <div>
 
       <h2>Reference</h2>
 
       <h2>Reference</h2>
 
+
      <ul>
 +
        <li>[1]Neupert J, Karcher D, Bock R. Design of simple synthetic RNA thermometers for temperature-controlled gene expression, in <i>Escherichia coli</i>.[J]. Nature Protocols, 2008, 4(9):1262-73.</li>
 +
  <li>[2]Kortmann J, Narberhaus F. Bacterial RNA thermometers: molecular zippers and switches.[J]. Nature Reviews Microbiology, 2012, 10(4):255-65.</li>
 +
  <li>[3]Neupert J, Bock R. Designing and using synthetic RNA thermometers for temperature-controlled gene expression in bacteria. Nature Protocols, 2009, 4(9):1262-73.</li>
 +
  <li>[4]Sen S, Apurva D, Satija R, et al. Design of a Toolbox of RNA Thermometers[J]. Acs Synthetic Biology, 2017, 6(8).</li>
 +
  <li>[5]Hoynes-O'Connor A, Hinman K, Kirchner L, et al. De novo design of heat-repressible RNA thermosensors in <i>E. coli</i>[J]. Nucleic Acids Research, 2015, 43(12):6166-6179.</li>
 +
  <li>[6]Pertzev A V, Nicholson A W. Characterization of RNA sequence determinants and antideterminants of processing reactivity for a minimal substrate of Escherichia coli ribonuclease III[J]. Nucleic Acids Research, 2006, 34(13):3708-3721.</li>
 +
  <li>[7]Giuliodori A M, Di P F, Marzi S, et al. The cspA mRNA is a thermosensor that modulates translation of the cold-shock protein CspA.[J]. Molecular Cell, 2010, 37(1):21-33.</li>
 +
  <li>[8]Breaker R R. RNA Switches Out in the Cold[J]. Molecular Cell, 2010, 37(1):1-2.</li>
 +
          <li>[9]Overkamp W, Beilharz K, Detert O W R, et al. Benchmarking various green fluorescent protein variants in Bacillus subtilis, Streptococcus pneumoniae, and Lactococcus lactis for live cell imaging.[J]. Applied & Environmental Microbiology, 2013, 79(20):6481-6490.</li>
 +
      </ul>
 
     </div>
 
     </div>
 
     </li>
 
     </li>

Latest revision as of 21:43, 17 October 2018

OVERVIEW
PARTS


Parts Overview

  • Introduction

    This year, Jilin_China build hundreds of parts, including 90 basic parts, 7 composite parts and 3 part collections. If you want to see more details, you can find the usage and characterization in the part registry page. You can also visit the basic part, composite part and part collection page for more information.

  • Parts

    <groupparts>iGEM18 Jilin_China</groupparts>
  • Reference

    • [1]Neupert J, Karcher D, Bock R. Design of simple synthetic RNA thermometers for temperature-controlled gene expression, in Escherichia coli.[J]. Nature Protocols, 2008, 4(9):1262-73.
    • [2]Kortmann J, Narberhaus F. Bacterial RNA thermometers: molecular zippers and switches.[J]. Nature Reviews Microbiology, 2012, 10(4):255-65.
    • [3]Neupert J, Bock R. Designing and using synthetic RNA thermometers for temperature-controlled gene expression in bacteria. Nature Protocols, 2009, 4(9):1262-73.
    • [4]Sen S, Apurva D, Satija R, et al. Design of a Toolbox of RNA Thermometers[J]. Acs Synthetic Biology, 2017, 6(8).
    • [5]Hoynes-O'Connor A, Hinman K, Kirchner L, et al. De novo design of heat-repressible RNA thermosensors in E. coli[J]. Nucleic Acids Research, 2015, 43(12):6166-6179.
    • [6]Pertzev A V, Nicholson A W. Characterization of RNA sequence determinants and antideterminants of processing reactivity for a minimal substrate of Escherichia coli ribonuclease III[J]. Nucleic Acids Research, 2006, 34(13):3708-3721.
    • [7]Giuliodori A M, Di P F, Marzi S, et al. The cspA mRNA is a thermosensor that modulates translation of the cold-shock protein CspA.[J]. Molecular Cell, 2010, 37(1):21-33.
    • [8]Breaker R R. RNA Switches Out in the Cold[J]. Molecular Cell, 2010, 37(1):1-2.
    • [9]Overkamp W, Beilharz K, Detert O W R, et al. Benchmarking various green fluorescent protein variants in Bacillus subtilis, Streptococcus pneumoniae, and Lactococcus lactis for live cell imaging.[J]. Applied & Environmental Microbiology, 2013, 79(20):6481-6490.