Difference between revisions of "Team:Aalto-Helsinki/Parts"

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{{Aalto-Helsinki/CSS}}
 
{{Aalto-Helsinki/CSS}}
 
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<style type="text/css">
  
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/* Navbar, text color changes if you are on this page */
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#resultsnav {
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</p></div>
 
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<ul id="sidenav" class="nav nav-stacked bottom"><!-- nav-pills if we want rounded corners -->
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        <li><a href="#" data-scroll="propane"><h3>Propane 1</h3></a></li>
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        <li><a href="#" data-scroll="gfp"><h3>Fusable GFP</h3></a></li>
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        <li><a href="#" data-scroll="amph"><h3>Amphiphilic</h3></a></li>
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        <li><a href="#" ><h3  style="border-top:solid;">To the top</h3></a></li>
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        <li><a href="https://2015.igem.org/Team:Aalto-Helsinki/Results" ><h3>To the Parent Page</h3></a></li>
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      </ul>
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<div class="proodlebg">
 
<div class="inner-container">
 
<div class="inner-container">
  
 
<h1>Submitted Parts</h1>
 
<h1>Submitted Parts</h1>
  
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<section id="propane" class="active" data-anchor="propane">
 
<h2>Propane 1</h2>
 
<h2>Propane 1</h2>
  
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<p>Our Propane 1 includes 4 of the 10 required genes to produce propane in <i>E. coli</i>. The plasmid has been assembled from IDT's gBlocks with NEBuilder assembly, similar to Gibson Assembly.</p>
 
<p>Our Propane 1 includes 4 of the 10 required genes to produce propane in <i>E. coli</i>. The plasmid has been assembled from IDT's gBlocks with NEBuilder assembly, similar to Gibson Assembly.</p>
 
<p><b>Validation:</b></p>  
 
<p><b>Validation:</b></p>  
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<h2>Fusable GFP</h2>
 
<h2>Fusable GFP</h2>
  
 
<p>We built a GFP biobrick which can be fused to any protein's aminoterminal end with the standard BioBrick assembly enzymes. We have added an extra nucleotide prior to the brick's suffix to maintain the reading frame after fusion, which is typically lost when the restriction enzyme assembly is used. </p>
 
<p>We built a GFP biobrick which can be fused to any protein's aminoterminal end with the standard BioBrick assembly enzymes. We have added an extra nucleotide prior to the brick's suffix to maintain the reading frame after fusion, which is typically lost when the restriction enzyme assembly is used. </p>
 
<p><b>Validation:</b> Our GFP brick has been fully sequenced, and the sequencing results were as expected. We have also been able to express the GFP after fusing it with an amphiphilic brick. This construct functioned under K608003, a strong constitutive promoter and a medium RBS. HS Slovenia Team also helped us validate this brick. They gained positive results of their construct with the GFP through colony PCR and analytical restrictions, but were unable to detect the fluerescence under UV light or functionality of the fused protein.</p>
 
<p><b>Validation:</b> Our GFP brick has been fully sequenced, and the sequencing results were as expected. We have also been able to express the GFP after fusing it with an amphiphilic brick. This construct functioned under K608003, a strong constitutive promoter and a medium RBS. HS Slovenia Team also helped us validate this brick. They gained positive results of their construct with the GFP through colony PCR and analytical restrictions, but were unable to detect the fluerescence under UV light or functionality of the fused protein.</p>
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<section id="amph" class="active" data-anchor="amph">
 
<h2>Amphiphilic</h2>
 
<h2>Amphiphilic</h2>
  
 
<p>We submitted a sole amphiphilic brick, containing only the coding region of the ampihphilic protein. This brick can be used to produce intracellular micelles or vesicles under any chosen expression system.</p>
 
<p>We submitted a sole amphiphilic brick, containing only the coding region of the ampihphilic protein. This brick can be used to produce intracellular micelles or vesicles under any chosen expression system.</p>
 
<p><b>Validation:</b> Our amphiphilic brick's sequencing results were unclear, as the brick is mainly built of short repeats. <span style="color:red">Microscope pictures!</span></p>
 
<p><b>Validation:</b> Our amphiphilic brick's sequencing results were unclear, as the brick is mainly built of short repeats. <span style="color:red">Microscope pictures!</span></p>
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<h2> Part Documentation</h2>
 
<h2> Part Documentation</h2>
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<script src="https://2015.igem.org/Team:Aalto-Helsinki/ResponsiveNavScript?action=raw&ctype=text/javascript"></script>
 
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Revision as of 08:39, 13 September 2015

Submitted Parts

Propane 1

Our Propane 1 includes 4 of the 10 required genes to produce propane in E. coli. The plasmid has been assembled from IDT's gBlocks with NEBuilder assembly, similar to Gibson Assembly.

Validation:

Fusable GFP

We built a GFP biobrick which can be fused to any protein's aminoterminal end with the standard BioBrick assembly enzymes. We have added an extra nucleotide prior to the brick's suffix to maintain the reading frame after fusion, which is typically lost when the restriction enzyme assembly is used.

Validation: Our GFP brick has been fully sequenced, and the sequencing results were as expected. We have also been able to express the GFP after fusing it with an amphiphilic brick. This construct functioned under K608003, a strong constitutive promoter and a medium RBS. HS Slovenia Team also helped us validate this brick. They gained positive results of their construct with the GFP through colony PCR and analytical restrictions, but were unable to detect the fluerescence under UV light or functionality of the fused protein.

Amphiphilic

We submitted a sole amphiphilic brick, containing only the coding region of the ampihphilic protein. This brick can be used to produce intracellular micelles or vesicles under any chosen expression system.

Validation: Our amphiphilic brick's sequencing results were unclear, as the brick is mainly built of short repeats. Microscope pictures!

Part Documentation

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 <groupparts> tag (see below) will generate a table with all of the parts that your team adds to your team sandbox.

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.

Note

Note that parts must be documented on the Registry. This page serves to showcase 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.

Adding parts to the registry

You can add parts to the Registry at our Add a Part to the Registry link.

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 do 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.)

What information do I need to start putting my parts on the Registry?

The information needed to initially create a part on the Registry is:

  • Part Name
  • Part type
  • Creator
  • Sequence
  • Short Description (60 characters on what the DNA does)
  • Long Description (Longer description of what the DNA does)
  • Design considerations

We encourage you to put up much more 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.

Inspiration

We have a created a collection of well documented parts that can help you get started.

You can also take a look at how other teams have documented their parts in their wiki:

Part Table

<groupparts>iGEM015 Example</groupparts>