Team:Hong Kong HKUST/experiment/exp2

From 2013.igem.org

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<br><br><br><div id="slide"><center><h3 class="title">Blogging Synthetic Biology</h3></center><br>  
<br><br><br><div id="slide"><center><h3 class="title">Blogging Synthetic Biology</h3></center><br>  
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<h3>Introduction</h3>
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<h1>BBa_J176171</h1>
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<p id="yo">For one of our human practice projects, our team investigated the current development of synthetic biology in some of the Asian countries. While doing research, we found out that synthetic biology is really a new field in science and that is not well-known in Asia. In fact, when some of our members tried to research information about synthetic biology in Cantonese, we could not find any webpages dedicated to share information about synthetic biology for the public in Hong Kong. To address this observation, we have decided to use an easily accessible platform called Google Blogger. This blog will be used as mean to introduce synthetic biology, share our experience and our project, and report current events related to synthetic biology. It will be written in Chinese and English so that most people in Hong Kong can read it easily and pay more attention to this new field in science. By providing holistic and informational blog posts, we aim at raising the public awareness to synthetic biology.</p><br>
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<p id="yo">BBa_ J176171 was planned to be used as a mammalian vector backbone for the promoters. After running PCR (Polymerase Chain Reaction) to amplify the FABP1 promoter and ligated it with GFP and the backbone, we did mutagenesis for the vector. Based on the gel photo, we concluded that the vector was easy to get degraded. Finally we figured out that BBa-J176171 was heat unstable and changed our plan.</p><br>
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<h3>A Sneak Peek of Our Blog</h3><br>
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<center><img src="https://static.igem.org/mediawiki/2013/2/2e/Blog-cecilia.png" style="width:90%"></center><br>
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<p id="hey">CLICK <a href="http://synbiohk.blogspot.hk">HERE</a> TO VISIT OUR BLOG! </p>
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Revision as of 18:45, 27 September 2013




Blogging Synthetic Biology


BBa_J176171

BBa_ J176171 was planned to be used as a mammalian vector backbone for the promoters. After running PCR (Polymerase Chain Reaction) to amplify the FABP1 promoter and ligated it with GFP and the backbone, we did mutagenesis for the vector. Based on the gel photo, we concluded that the vector was easy to get degraded. Finally we figured out that BBa-J176171 was heat unstable and changed our plan.