Difference between revisions of "Team:MIT/Human Practices"
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| − | <a href="https://2016.igem.org/Team:MIT/Mammalian_synthetic_biology_kit"><h1 style="background-color:#7ecefd;; -moz-border-radius: 15px; -webkit-border-radius: 15px; padding:15px; text-align: center; font-family: Trebuchet MS"> Making Mammalian Synthetic Biology Accessible </h1> </a> | + | <a href="https://2016.igem.org/Team:MIT/Mammalian_synthetic_biology_kit"><h1 style="color:#000000; background-color:#7ecefd;; -moz-border-radius: 15px; -webkit-border-radius: 15px; padding:15px; text-align: center; font-family: Trebuchet MS"> Making Mammalian Synthetic Biology Accessible </h1> </a> |
<h2> Mammalian SynBio Toolkit: pDest-mCherry and Parts Collection </h2> | <h2> Mammalian SynBio Toolkit: pDest-mCherry and Parts Collection </h2> | ||
<p style="font-family:Verdana;"> We created a destination plasmid with a fluorescent protein selection marker that can be used for cloning mammalian parts. We submitted a collection of well-characterized mammalian parts to the registry, in hopes that this will help future iGEM teams work in mammalian synthetic biology. | <p style="font-family:Verdana;"> We created a destination plasmid with a fluorescent protein selection marker that can be used for cloning mammalian parts. We submitted a collection of well-characterized mammalian parts to the registry, in hopes that this will help future iGEM teams work in mammalian synthetic biology. | ||
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| − | <a href="https://2016.igem.org/Team:MIT/Engagement"><h1 style="background-color:#7ecefd;; -moz-border-radius: 15px; -webkit-border-radius: 15px; padding:15px; text-align: center; font-family: Trebuchet MS"> Public Outreach & Engagement </h1> </a> | + | <a href="https://2016.igem.org/Team:MIT/Engagement"><h1 style="color:#000000; background-color:#7ecefd;; -moz-border-radius: 15px; -webkit-border-radius: 15px; padding:15px; text-align: center; font-family: Trebuchet MS"> Public Outreach & Engagement </h1> </a> |
<p style="font-family:Verdana;"> Through both presentations and social media, we were able to share our work with a variety of audiences, from young children and their parents to experienced industry scientists, and educate the public about both synthetic biology and endometriosis. Here are some of our accomplishments: | <p style="font-family:Verdana;"> Through both presentations and social media, we were able to share our work with a variety of audiences, from young children and their parents to experienced industry scientists, and educate the public about both synthetic biology and endometriosis. Here are some of our accomplishments: | ||
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Revision as of 17:45, 9 October 2016
Making Mammalian Synthetic Biology Accessible
Mammalian SynBio Toolkit: pDest-mCherry and Parts Collection
We created a destination plasmid with a fluorescent protein selection marker that can be used for cloning mammalian parts. We submitted a collection of well-characterized mammalian parts to the registry, in hopes that this will help future iGEM teams work in mammalian synthetic biology.
Protocols for Mammalian SynBio
One of our team members documented many common mammalian synthetic biology protocols, and created a website to help visualize these steps.
Public Outreach & Engagement
Through both presentations and social media, we were able to share our work with a variety of audiences, from young children and their parents to experienced industry scientists, and educate the public about both synthetic biology and endometriosis. Here are some of our accomplishments:
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Building with Biology
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Online Articles about Endometriosis and iGEM
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Industry Visits
