Difference between revisions of "Team:TU Delft/Parts"

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             <div class="container">
 
             <div class="container">
 
                 <h1 class="page-header">Parts<span class="title-under"></span></h1>
 
                 <h1 class="page-header">Parts<span class="title-under"></span></h1>
 +
                <p>For the construction of our parts, we made use of the IDT synthesis offer. This way we were able to
 +
                            generate our required parts in a fast and efficient way. All of the parts were designed containing the coding
 +
                            sequence, RBS, promoter and terminators, if applicable. Therefore, all of the parts we used are <a href="#composite"><b>composite</b></a>.
 +
                            The different <a href="#basic"><b>basic</b></a> parts comprising the composite parts are documented seperately, although they do not exist induvidually.</p>
 +
                            <p>In the case of a constitutive expression, the promoter is included in the biobrick itself.
 +
                            For the inducible expression, however, we made use of a plasmid backbone containing a Lac-promoter
 +
                            and the LacI gene, which encodes for the Lac repressor. Consequently, these parts themselves do
 +
                            not contain a promoter.</p>
 +
                            <p>Additionally, using PCR rather than synthesis, we constructed a small
 +
                                <a href="#collection"><b>collection</b></a> of GFP expression devices, based on an existing biobrick.</p>
 +
                           
 
             </div>
 
             </div>
 
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                         <h2 class="title-style-1">All Parts<span class="title-under"></span></h2>
 
                         <h2 class="title-style-1">All Parts<span class="title-under"></span></h2>
 
                         <div class="container">
 
                         <div class="container">
                            <p>For the construction of our parts, we made use of the IDT synthesis offer. This way we were able to
 
                            generate our required parts in a fast and efficient way. All of the parts were designed containing the coding
 
                            sequence, RBS, promoter and terminators, if applicable. Therefore, all of the parts we used are <a href="#composite"><b>composite</b></a>.
 
                            The different <a href="#basic"><b>basic</b></a> parts comprising the composite parts are documented seperately, although they do not exist induvidually.</p>
 
                            <p>In the case of a constitutive expression, the promoter is included in the biobrick itself.
 
                            For the inducible expression, however, we made use of a plasmid backbone containing a Lac-promoter
 
                            and the LacI gene, which encodes for the Lac repressor. Consequently, these parts themselves do
 
                            not contain a promoter.</p>
 
                            <p>Additionally, using PCR rather than synthesis, we constructed a small
 
                                <a href="#collection"><b>collection</b></a> of GFP expression devices, based on an existing biobrick.</p>
 
 
                             <div class="col-md-6 col-md-offset-2">
 
                             <div class="col-md-6 col-md-offset-2">
 
                                 </html>
 
                                 </html>

Revision as of 07:45, 16 October 2016

iGEM TU Delft

Parts

For the construction of our parts, we made use of the IDT synthesis offer. This way we were able to generate our required parts in a fast and efficient way. All of the parts were designed containing the coding sequence, RBS, promoter and terminators, if applicable. Therefore, all of the parts we used are composite. The different basic parts comprising the composite parts are documented seperately, although they do not exist induvidually.

In the case of a constitutive expression, the promoter is included in the biobrick itself. For the inducible expression, however, we made use of a plasmid backbone containing a Lac-promoter and the LacI gene, which encodes for the Lac repressor. Consequently, these parts themselves do not contain a promoter.

Additionally, using PCR rather than synthesis, we constructed a small collection of GFP expression devices, based on an existing biobrick.

All Parts

                               <groupparts class="parts">iGEM2016 TU_Delft</groupparts>
                               
                            

Composite Parts

Name Type Description Designer Length
BBa_K1890000 Composite Silicatein gene with strong RBS Lycka Kamoen, Maria Vazquez 686
BBa_K1890001 Composite Silicatein gene, fused to transmembrane domain of INP, with strong RBS Lycka Kamoen, Maria Vazquez 1442
BBa_K1890002 Composite Silicatein gene, fused to transmembrane domain of OmpA, with strong RBS Lycka Kamoen, Maria Vazquez 1481
BBa_K1890010 Composite mCerulean with strong consitutive promoter and RBS Lycka Kamoen, Maria Vazquez 784
BBa_K1890011 Composite mVenus with strong consitutive promoter and RBS Lycka Kamoen, Maria Vazquez 784
BBa_K1890020 Generator GFP with strong constitutive promoter, RBS and terminator Lycka Kamoen, Maria Vazquez 913
BBa_K1890021 Generator GFP with strong constitutive promoter, RBS and terminator Lycka Kamoen, Maria Vazquez 913
BBa_K1890022 Generator GFP with medium constitutive promoter, RBS and terminator Lycka Kamoen, Maria Vazquez 913
BBa_K1890023 Generator GFP with weak constitutive promoter, RBS and terminator Lycka Kamoen, Maria Vazquez 913
BBa_K1890024 Generator GFP with weak constitutive promoter, RBS and terminator Lycka Kamoen, Maria Vazquez 913
BBa_K1890030 Composite BolA gene with RBS and terminator Lycka Kamoen, Maria Vazquez 508
BBa_K1890031 Composite BolA gene with strong promoter, RBS and terminator Lycka Kamoen, Maria Vazquez 519

Basic Parts

Part Collection

We provided a small collection of GFP expression divices with different promoter strengths, which we used to study the effect of constitutive expression. These parts are ready-to-go expression units for green fluorescence, which can be usefull for future teams.

Name Type Description Designer Length
BBa_K1890020 Generator GFP with strong constitutive promoter, RBS and terminator Lycka Kamoen, Maria Vazquez 913
BBa_K1890021 Generator GFP with strong constitutive promoter, RBS and terminator Lycka Kamoen, Maria Vazquez 913
BBa_K1890022 Generator GFP with medium constitutive promoter, RBS and terminator Lycka Kamoen, Maria Vazquez 913
BBa_K1890023 Generator GFP with weak constitutive promoter, RBS and terminator Lycka Kamoen, Maria Vazquez 913
BBa_K1890024 Generator GFP with weak constitutive promoter, RBS and terminator Lycka Kamoen, Maria Vazquez 913