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<p> Had our first investor presentation with BioMatters! They were really receptive towards our idea in terms of it being relevant to nitrogen pollution in New Zealand. Such a cool experience connecting with people in the industry who are equally passionate about GMOs and are keen to support us! </p> | <p> Had our first investor presentation with BioMatters! They were really receptive towards our idea in terms of it being relevant to nitrogen pollution in New Zealand. Such a cool experience connecting with people in the industry who are equally passionate about GMOs and are keen to support us! </p> | ||
<p>Had our investor pitch with Return On Science! It’s cool to see our lab students present the entrepreneurial aspects of our project for the first time. We got some good feedback on areas of commercialization we should deeper look into - particularly around IP and our business model. </p> | <p>Had our investor pitch with Return On Science! It’s cool to see our lab students present the entrepreneurial aspects of our project for the first time. We got some good feedback on areas of commercialization we should deeper look into - particularly around IP and our business model. </p> | ||
− | <img src="https:// | + | <img src="https://2018.igem.org/File:T--Auckland_MOD--BiomattersPresentation.jpeg"> |
<h4>Working through the BioBrick lab</h4> | <h4>Working through the BioBrick lab</h4> | ||
<p>We’ve successfully transformed our composite RFP BioBrick into E. coli and run colony PCR to confirm. We’ll be spending the rest of the week planning our purification technique (subcloning into another vector to add a HisTag) and fluorescent characterization under different salinities. We’ve found the transformed E. coli grow a bit slower than usual - we’ll be asking past teams that have worked with our BioBrick if they’ve encountered the same problems.</p> | <p>We’ve successfully transformed our composite RFP BioBrick into E. coli and run colony PCR to confirm. We’ll be spending the rest of the week planning our purification technique (subcloning into another vector to add a HisTag) and fluorescent characterization under different salinities. We’ve found the transformed E. coli grow a bit slower than usual - we’ll be asking past teams that have worked with our BioBrick if they’ve encountered the same problems.</p> |
Revision as of 02:49, 19 July 2018
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"Competing in iGEM required more strength, endurance, and sacrifice than any other project I have undertaken. But nothing could have prepared me more for the post graduate study I am now pursuing than formulating and completing our project as an independent scienctist."
Judith Glasson, Alumni
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