Difference between revisions of "Team:TUDelft/Part Collection"

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<h3>★  ALERT! </h3>
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<p>This page is used by the judges to evaluate your team for the <a href="https://2018.igem.org/Judging/Medals">medal criterion</a> or <a href="https://2018.igem.org/Judging/Awards"> award listed below</a>. </p>
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<p> Delete this box in order to be evaluated for this medal criterion and/or award. See more information at <a href="https://2018.igem.org/Judging/Pages_for_Awards"> Instructions for Pages for awards</a>.</p>
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<h1> Part Collection </h1>
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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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While you should put all the characterization information for your parts on the Registry, you are encouraged to explain how all your parts form a collection on this page.
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<h3>Note</h3>
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<p>This page should list all the parts in the collection your team made during your project. You must add all characterization information for your parts on the Registry. You should not put characterization information on this page.</p>
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<h3>Best Part Collection Special Prize</h3>
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<p>To be eligible for this award, these parts must adhere to <a href="http://parts.igem.org/DNA_Submission">Registry sample submission guidelines</a> and have been sent to the Registry of Standard Biological Parts. If you have a collection of parts you wish to nominate your team for this <a href="https://2018.igem.org/Judging/Awards">special prize</a>, make sure you add your part numbers to your <a href="https://2018.igem.org/Judging/Judging_Form">judging form</a> and delete the box at the top of this page.</p>
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Revision as of 14:28, 10 September 2018

ADOPE

partcollection

Part Collection

When constructing our BioBricks, we made use of the IDT synthesis offer. This way we were able to generate our required parts in a fast and efficient way. Additionally, we made use of PCR amplification with our constructed expression plasmids as template to construct several BioBricks. We created a part collection comprised of 6 basic parts encoding for different EPO coding sequences, 2 basic parts encoding for the required components for targeted sequencing and 1 composite part: our fusion protein. All BioBricks are submitted with elaborate characterisation so the user may choose the best protein for their project accordingly.

Our part collection establishes a platform for Targeted Next Generation Sequencing applicable for gene doping detection. Additionally, this part collection can easily be applied to any scientific case that requires analysis of specific sequences. The platform includes a transposase-dxCas9 fusion protein, transposon adapter sequence, sgRNA sequence, and multiple target and off-target EPO sequences. These components are required to perform RNA-guided adapter ligation needed for target specific sequencing. As a result, the technology can rapidly process the specific DNA sequence of interest, minimizing data output and sequencing time. The part collection also contains an adapter sequence containing an example barcode. Barcoding different samples allows for multiplexing, increasing the number of samples sequenced simultaneously. Our part collection sets the basis for targeted next generation sequencing by providing all necessary components, adjustable at will, and can be a solution in almost any sequencing case.

Table 1. BioBrick Parts composing the Part Collection submitted by TU Delft iGEM 2018 team. All BioBricks were constructed by the team members involved in wetlab: Susan Bouwmeester, Kavish Kohabir, Venda Mangkusaputra, Timmy Paez, Lisbeth Schmidtchen and Nicole Bennis
Name Type Description Designer
BBa_K2643000 Composite dxCas9-linker-Tn5 fusion protein (HIS Tag) TU Delft 2018
BBa_K2643004 Basic Coding region (CDS) of human erythropoietin (EPO) hormone TU Delft 2018
BBa_K2643005 Basic Human EPO gene with artificial intron (615 bp) TU Delft 2018
BBa_K2643006 Basic Human EPO gene with artificial intron (135 bp) TU Delft 2018
BBa_K2643007 Basic Human EPO gene with 2 artificial introns (615 + 135 bp) TU Delft 2018
BBa_K2643008 Basic Human EPO gene with mutation 1 (5 bp) TU Delft 2018
BBa_K2643009 Basic Human EPO gene with mutation 2 (12 bp) TU Delft 2018
BBa_K2643011 Basic Mosaic Ends-flanked Kanamycin cassette and RFP TU Delft 2018
BBa_K2643012 Basic T7p expressing sgRNA targeting the EPO coding sequence TU Delft 2018