Team:MIT/Results
From 2012.igem.org
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+ | <b>In Vivo RNA Strand Displacement </b> | ||
+ | <br> | ||
+ | <br> | ||
+ | <b> Strategy 1: Take DNA sequences that worked in In Vitro Strand Displacement, convert to RNA, transfect inside HEK293 cells </b> | ||
+ | <br> | ||
+ | <br> | ||
+ | <b> Strategy 2: Tag RNA strand with an Alexa Fluorophore to act as a transfection marker </b> | ||
+ | <br> | ||
+ | <br> | ||
+ | <b> Strategy 3: Create DNA plasmids driving transcription of RNA inputs, while transfecting RNA Reporter </b> | ||
+ | <br> | ||
+ | <br> | ||
+ | <b> Strategy 4: Nucleofect RNA reporter, RNA inputs </b> | ||
+ | <br> | ||
+ | <br> | ||
+ | <b> [[Strategy 5]]: Redesign RNA Reporter </b> | ||
</div> | </div> | ||
Revision as of 04:23, 25 September 2012
RNA Strand Displacement In Vitro
Nucleic Acid Delivery
In Vivo RNA Strand Displacement
Strategy 1: Take DNA sequences that worked in In Vitro Strand Displacement, convert to RNA, transfect inside HEK293 cells
Strategy 2: Tag RNA strand with an Alexa Fluorophore to act as a transfection marker
Strategy 3: Create DNA plasmids driving transcription of RNA inputs, while transfecting RNA Reporter
Strategy 4: Nucleofect RNA reporter, RNA inputs
[[Strategy 5]]: Redesign RNA Reporter
Strategy 1: Take DNA sequences that worked in In Vitro Strand Displacement, convert to RNA, transfect inside HEK293 cells
Strategy 2: Tag RNA strand with an Alexa Fluorophore to act as a transfection marker
Strategy 3: Create DNA plasmids driving transcription of RNA inputs, while transfecting RNA Reporter
Strategy 4: Nucleofect RNA reporter, RNA inputs
[[Strategy 5]]: Redesign RNA Reporter