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<h1 style="color:#000000; background-color:#FF9733; -moz-border-radius: 15px; -webkit-border-radius: 15px; padding:15px; text-align: center"> General Experimental Set-Up and Data Analysis </h1> | <h1 style="color:#000000; background-color:#FF9733; -moz-border-radius: 15px; -webkit-border-radius: 15px; padding:15px; text-align: center"> General Experimental Set-Up and Data Analysis </h1> | ||
<h2 style="color:#000000;text-decoration:underline"> miRNA Sensor </h2> | <h2 style="color:#000000;text-decoration:underline"> miRNA Sensor </h2> | ||
− | <a href=https://2016.igem.org/Team:MIT/Experiments/miRNA/more_background>Read about here</a> | + | <a href=https://2016.igem.org/Team:MIT/Experiments/miRNA/more_background>Read about here</a> |
<p></p> | <p></p> | ||
<br> | <br> |
Revision as of 19:17, 16 October 2016
General Experimental Set-Up and Data Analysis
miRNA Sensor
Read about hereTransient Transfection
Flow Cytometry Analysis
Sensitivity of miRNA Target Sites
Purpose
We want to understand the sensitivity of our miRNA target site constructs.
Set Up
We chose one miRNA target site, 451a, and designed and ordered siRNA complementary to the target site. We co-transfected tert-immortalized human endometrial stromal cells with our miRNA sensors and varying concentrations of siRNA then measured the red fluorescence output to gauge repression.
Results
When increasing siRNA-451a 0 to 1 nM, there is a 10 fold repression of red fluorescence. Saturation occurs at approximately 10 nM. More experiments would need to be done to understand the responsiveness between 0 to 1 nM.
miRNA Profile of tHESC
Purpose
Set Up