Difference between revisions of "Team:Peking/Parts"
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<li class="menunew"><a href="#List">Part list</a></li> | <li class="menunew"><a href="#List">Part list</a></li> | ||
<li class="menunew"><a href="#Basic">Basic Parts</a></li> | <li class="menunew"><a href="#Basic">Basic Parts</a></li> | ||
| + | <li class="menunew"><a href="#Composite">Composite Parts</a></li> | ||
<li class="menunew"><a href="#Collection">Parts Collection</a></li> | <li class="menunew"><a href="#Collection">Parts Collection</a></li> | ||
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<img alt="Part image" src="http://parts.igem.org/wiki/images/f/f7/T--Peking--dCas9-ssrA.png" style="width:30%;"> | <img alt="Part image" src="http://parts.igem.org/wiki/images/f/f7/T--Peking--dCas9-ssrA.png" style="width:30%;"> | ||
<img alt="Part image" src="http://parts.igem.org/wiki/images/9/96/T--Peking--PBAD-dCas9-J23119-M%2B.png" style="width:80%;"> | <img alt="Part image" src="http://parts.igem.org/wiki/images/9/96/T--Peking--PBAD-dCas9-J23119-M%2B.png" style="width:80%;"> | ||
| + | </div> | ||
| + | <div class="column full_size" style="width: 70%; float: right;"> | ||
| + | <div class="clear extra_space" id="Composite"></div> | ||
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| + | <div class="clear extra_space"></div> | ||
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| + | <h1>Favorite Parts</h1> | ||
| + | <div class="clear line_divider"></div> | ||
| + | <img alt="Part image" src="https://2019.igem.org/wiki/images/6/60/T--Peking--m%2B.gif" style="width:20%;"> | ||
| + | <div style="width: 100%;"> | ||
| + | <p>part description</p> | ||
| + | </div> | ||
</div> | </div> | ||
Revision as of 20:25, 20 October 2019
Parts List
| Part Name | Part Type | Description |
|---|---|---|
| BBa_K3081104 | RNA | gRNA scaffold |
| BBa_K3081105 | RNA | sgRNA |
| BBa_K3081106 | RNA | polyA |
| BBa_K3081107 | RNA | M+ |
| BBa_K3081108 | RNA | R1+ |
| BBa_K3081109 | RNA | R1+ (18bp) |
| BBa_K3081110 | RNA | R1+ (19bp) |
| BBa_K3081111 | RNA | R1- |
| BBa_K3081112 | RNA | R4- |
| BBa_K3081113 | RNA | MR13 |
| BBa_K3081114 | RNA | IHF |
| BBa_K3081115 | RNA | R3+ |
| BBa_K3081116 | RNA | M-R2+ |
| BBa_K3081120 | RNA | pL01 |
| BBa_K3081121 | RNA | pL05 |
| BBa_K3081119 | coding | dCas9-linker-sfGFP |
| BBa_K3081122 | coding | dCas9-linker-sfGFP ssrA |
| BBa_K3081060 | composite | A double-input CRISPRi system with tunable dCas9 and sgRNA targeting low-affinity DnaA box(M+) |
| BBa_K3081058 | composite | pBAD-dCas9-J23119-sgRNA |
| BBa_K3081006 | composite | pBAD-dCas9-J23119-polyA |
| BBa_K3081007 | composite | pBAD-dCas9-J23119-M+ |
| BBa_K3081008 | composite | pBAD-dCas9-J23119-R1+ |
| BBa_K3081009 | composite | pBAD-dCas9-J23119-R1+(18bp) |
| BBa_K3081010 | composite | pBAD-dCas9-J23119-R1+(19bp) |
| BBa_K3081011 | composite | pBAD-dCas9-J23119-R1- |
| BBa_K3081012 | composite | pBAD-dCas9-J23119-R4- |
| BBa_K3081013 | composite | pBAD-dCas9-J23119-MR13 |
| BBa_K3081014 | composite | pBAD-dCas9-J23119-IHF |
| BBa_K3081015 | composite | pBAD-dCas9-J23119-R3+ |
| BBa_K3081016 | composite | pBAD-dCas9-J23119-M-R2+ |
| BBa_K3081031 | composite | pBAD-dCas9-ssrA-J23119-R1+ |
| BBa_K3081024 | composite | pBAD-dCas9-J23119-NT1-J23119-mRFP |
| BBa_K3081027 | composite | pBAD-dCas9-J23119-M+-J23119-R1+ |
| BBa_K3081057 | composite | pBAD-dCas9-ssrA-J23119-p15A-initiation(+) |
| BBa_K3081041 | composite | pBAD-dCas9-ssrA-J23119-p15A-initiation(-) |
| BBa_K3081042 | composite | pBAD-dCas9-ssrA-J23119-p15A-primer NT |
| BBa_K3081043 | composite | pBAD-dCas9-ssrA-J23119-p15A-RNA I NT |
| BBa_K3081044 | composite | pBAD-dCas9-J23119-ssrA-NT1-J23119-mRFP |
| BBa_K3081059 | composite | TcI42-dCas9-J23119-M+ |
| BBa_K3081061 | composite | TcI42-dCas9-J23119-polyA |
| composite | des | |
| composite | des |
Basic Parts
Favorite Parts
part description
Part Collection
2019 Peking iGEM constructed a large part collection focusing on dCas9-based DNA replication control. The dCas9 expression module has been optimized and expanded by using different regulatory elements, adding degradation tag, fusing a fluorescent protein reporter, etc. The updated modules enable our system to function in a low-leakage, quantifiable and reversible manner, and a series of application scenarios. We also designed a new expression module for sgRNA. The new expression system of two inputs not only benefit our project but also can be a new paradigm of CRISPRi for subsequent researchers. We have also constructed a library of sgRNA to target the replication origin of E. coli genome or plasmids (p15A and pSC101). sgRNAs are different in target sites, length and number, thus can perform a wide range of control effects. All the parts are thoroughly characterized by different methods: microscopic imaging, spectrophotometer, cytometer, microfluidic devices, qPCR, etc.