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Commit cb4d2ce2 authored by Lucy Hao's avatar Lucy Hao :moyai:
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......@@ -29,7 +29,7 @@ export default function PillarsLanding() {
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To aid with our cell frree platform development, we designed an
To aid with our cell free platform development, we designed an
aerated bioreactor to culture our strain of <i>Vibrio natriegens</i>{" "}
for cell extract production.{" "}
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......@@ -42,7 +42,7 @@ To complement our wet lab, our team has designed a simple, easy to build and mos
At UBC iGEM, we strive to make content easily digestible and accessible to all, even those who may not be well versed in synthetic biology. We understand the three plasmid systems we have employed for protein purification, production and energy efficiency. Therefore, we have designed and written up an informative and extensive user manual that carefully details the pillars of our projects and their uses. This manual is intended to let future teams and users who may continue developing our toolkit for their purposes by carefully documenting the protocol and procedures we used in the project, safety considerations, and visions for scaled up use.
Finally, our well detailed protocols set contains extensive information on techniques use din the project. Since working with _Vibrio natriegens_ uses a slightly different set of techniques, we have a section documenting that as well. Finally, we have extensive protocols written on preparing bacterial cell lysate and running cell free protein synthesis (CFPS) reactions that have been buffer optimized. We have included exact concentrations used that have resulted in successful CFPS runs and we hope that this information comes useful to researchers in the future. For more information, you can find this on the User Manual page and the Protocols Page.
Finally, our well detailed protocols set contains extensive information on techniques use din the project. Since working with _Vibrio natriegens_ uses a slightly different set of techniques, we have a section documenting that as well. Finally, we have extensive protocols written on preparing bacterial cell lysate and running cell free protein synthesis (CFPS) reactions that have been buffer optimized. We have included exact concentrations used that have resulted in successful CFPS runs and we hope that this information comes useful to researchers in the future. For more information, you can find this on the [User Manual](/ubc-vancouver/usermanual) page and the [Protocols](/ubc-vancouver/protocols) Page.
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