Difference between revisions of "Team:Hong Kong HKU/Parts"

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<p> As shown before the Pre-tetra and the Tetra is generated using five nucleotide sequence and we have made a total of 5 biobricks, one biobrick for each. </p>  
 
<p> As shown before the Pre-tetra and the Tetra is generated using five nucleotide sequence and we have made a total of 5 biobricks, one biobrick for each. </p>  
 
   
 
   
<img src="https://static.igem.org/mediawiki/parts/b/ba/Plasmidconstruct1.png" alt="plasmidconstruct", style="width="800" height="800" " >
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<img src="https://static.igem.org/mediawiki/parts/b/ba/Plasmidconstruct1.png" alt="plasmidconstruct" style="width="800" height="800" " >
  
  

Revision as of 01:44, 29 October 2017



Parts

This year we produced 5 biobricks each of which produce ssDNA which can come together to form a functional tetrahedron structure in presence of its target. The inserts were ordered as gBlocks fragments from Integrated DNA technologies As shown in the diagram, the insert can be divided into 5 parts:

  1. Biobrick prefix and suffix
  2. ProD - This is the Promoter for our biobrick. The promoter allows for high expression of our downstream product
  3. ssDNA sequence: This sequence is complementary to the ncRNA sequence that will be produced.
  4. HTBS: HIV reverse transcriptase binding site
  5. BBa_B0054 : Strong Terminator

We expect that upon transcription a ncRNA will be produced with an HTBS sequence that will allow HIV reverse transcriptase to bind the ncRNA and produce the desired DNA sequence. Upon addition of RNase H and RNase A the DNA: RNA duplex and the degradation can occur respectively.

As shown before the Pre-tetra and the Tetra is generated using five nucleotide sequence and we have made a total of 5 biobricks, one biobrick for each.

plasmidconstruct <groupparts>iGEM17 Hong_Kong_HKU</groupparts>