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Team:NYMU-Taipei/Our institute
From 2010.igem.org
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| - | *'''<font size=3>Our design | + | *'''<font size=3>Our design</font>'''<br> |
| - | To achieve our specific aim, we have designed a novel reporting | + | To achieve our specific aim, we have designed a novel reporting device [[Team:NYMU-Taipei/Project/Speedy reporter|(Speedy reporter)]] for quickly detectin and measuring the mRNA location and quantity, it can also be used for protein detection. And we design a novel switch [[Team:NYMU-Taipei/Project/Speedy switch|(Speedy switch)]] for control the mRNA translation of gene expression. We have also designed a faster degradation device [[Team:NYMU-Taipei/Project/Speedy protein degrader |(Speedy protein degrader)]]; it allows us to regulate the degradation time for studying the mRNAs without the interference from translation and quickly stopping the gene expression.<br> |
| - | ''' | + | <br> |
| + | '''Our SpeedyBac system is made up of the following three devices''':<br> | ||
* [[Team:NYMU-Taipei/Project/Speedy switch | Speedy switch]] | * [[Team:NYMU-Taipei/Project/Speedy switch | Speedy switch]] | ||
| - | ** Faster production of protein by inducing the translation of pre- | + | ** Faster production of protein by inducing the translation of pre-existing mRNA molecules. |
* [[Team:NYMU-Taipei/Project/Speedy reporter| Speedy reporter]] | * [[Team:NYMU-Taipei/Project/Speedy reporter| Speedy reporter]] | ||
| - | ** Using mRNA aptamers and split GFP-eIF4A reporter | + | ** Using mRNA aptamers and split GFP-eIF4A reporter designs to detect promoter activity faster. |
* [[Team:NYMU-Taipei/Project/Speedy protein degrader | Speedy protein degrader]] | * [[Team:NYMU-Taipei/Project/Speedy protein degrader | Speedy protein degrader]] | ||
| - | ** Fast, specific, and constitutive proteolysis achieved by engineering fluorescent proteins with LVA | + | ** Fast, specific, and constitutive proteolysis achieved by engineering fluorescent proteins tagged with LVA |
| - | + | <br> | |
| - | *'''[[Team:NYMU-Taipei/Our institute|Our institute]]''' | + | *'''<font size=3>[[Team:NYMU-Taipei/Our institute|Our institute]]</font>''' |
| - | + | The official web pages of our school - National Yang Ming University (NYMU): | |
* [http://web.ym.edu.tw/front/bin/home.phtml in Chinese] | * [http://web.ym.edu.tw/front/bin/home.phtml in Chinese] | ||
* [http://nymu-e.web.ym.edu.tw/front/bin/home.phtml in English] | * [http://nymu-e.web.ym.edu.tw/front/bin/home.phtml in English] | ||
Latest revision as of 18:32, 27 October 2010
- Our design
To achieve our specific aim, we have designed a novel reporting device (Speedy reporter) for quickly detectin and measuring the mRNA location and quantity, it can also be used for protein detection. And we design a novel switch (Speedy switch) for control the mRNA translation of gene expression. We have also designed a faster degradation device (Speedy protein degrader); it allows us to regulate the degradation time for studying the mRNAs without the interference from translation and quickly stopping the gene expression.
Our SpeedyBac system is made up of the following three devices:
- Speedy switch
- Faster production of protein by inducing the translation of pre-existing mRNA molecules.
- Speedy reporter
- Using mRNA aptamers and split GFP-eIF4A reporter designs to detect promoter activity faster.
- Speedy protein degrader
- Fast, specific, and constitutive proteolysis achieved by engineering fluorescent proteins tagged with LVA
- Our institute
The official web pages of our school - National Yang Ming University (NYMU):
- [http://web.ym.edu.tw/front/bin/home.phtml in Chinese]
- [http://nymu-e.web.ym.edu.tw/front/bin/home.phtml in English]
Click the following two links to see The Beauty of NYMU
- [http://issue.ym.edu.tw/cia/new/ Take a panoramic scenery view of our university]
- [http://issue.ym.edu.tw/cia/new/tw/ym720.html Take a tour of our university]
