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Team:Calgary/Notebook/Protocols/GelShiftAssay
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<h2>Reagents and Materials</h2> | <h2>Reagents and Materials</h2> | ||
<ul> | <ul> | ||
| - | <li>1.3% <a href="https://2013.igem.org/Team:Calgary/Notebook/Protocols/AgaroseGelElectrophoresis">agarose gel</a></li> | + | <li>1.3% <a href="https://2013.igem.org/Team:Calgary/Notebook/Protocols/AgaroseGelElectrophoresis" target="_blank">agarose gel</a></li> |
<li>DNA of interest</li> | <li>DNA of interest</li> | ||
<li>Purified protein sample</li> | <li>Purified protein sample</li> | ||
Revision as of 00:54, 28 September 2013
Gel Shift Assay
Gel Shift Assay
Reagents and Materials
- 1.3% agarose gel
- DNA of interest
- Purified protein sample
10x Buffer
- 120mM Tris Cl
- 600mM KCl
- 20mM DTT
- 0.5% NP-40
- 1mg/mL BSA
- 50% Glycerol
- 50 mM MgCl2
- 2mM EDTA
- ddH2O (deionized water)
- pH = 7.5
Protocol
- Perform a Bradford Assay to the protein concentration
- Add 2µL of 10X Buffer, 55pM of DNA, 0.01 to 2500nM of Protein, and fill up to 20µL with ddH2O. Mix thoroughly
- Incubate for 1 hour at room temperature in the dark
- Place at 4°C for 30 minutes
- Run on a 1.3% agarose gel at 50V
