Difference between revisions of "20.109(F07):Module 2"
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[[20.109(F07): siRNA design | Module 2 Day 1: siRNA design and introduction to cell culture]]<br> | [[20.109(F07): siRNA design | Module 2 Day 1: siRNA design and introduction to cell culture]]<br> | ||
− | [[20.109(F07): Transfection | Module 2 Day 2: | + | [[20.109(F07): Transfection | Module 2 Day 2: Transfection]]<br> |
+ | [[20.109(F07): Luciferase assays and RNA prep| Module 2 Day 3: Luciferase assays and RNA prep]]<br> | ||
[[20.109(F07): Module 2 oral presentations| Module 2 Day 8: Oral Presentations]]<br> | [[20.109(F07): Module 2 oral presentations| Module 2 Day 8: Oral Presentations]]<br> | ||
Revision as of 01:32, 18 July 2007
Module 2
Instructors: Natalie Kuldell and Agi Stachowiak
TA: Alice Lo
In this experiment, we will consider unintended and unpredicted effects of an experimental perturbation. Our goal is a precise one, namely to silence gene expression of a measurable gene, luciferase, using RNA interference (RNAi). Each group will begin by designing a short interfering RNA (siRNA) against luciferase, but as we'll see, siRNAs can vary in efficacy and specificity. After transfecting a mammalian cell line with the siRNA you’ve designed and a reporter plasmid, we will evaluate the silencing using a luciferase assay and microarray technology. The first assay evaluates the efficacy of the siRNA in silencing. The second assay gives genome-wide expression data to reveal the specificity of your siRNA for the gene you’ve targeted. Through this combined approach, we'll assess the balance of targeted and off-target effects.
Module 2 Day 1: siRNA design and introduction to cell culture
Module 2 Day 2: Transfection
Module 2 Day 3: Luciferase assays and RNA prep
Module 2 Day 8: Oral Presentations