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Team:Calgary/Notebook/Protocols/GelShiftAssay
From 2013.igem.org
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<li>Purified protein sample</li> | <li>Purified protein sample</li> | ||
</ul> | </ul> | ||
| - | <p class="noIndent"><b>10x Buffer</b></p> | + | <p class="noIndent"><b>10x TALE binding Buffer</b></p> |
<ul> | <ul> | ||
<li>120mM Tris Cl</li> | <li>120mM Tris Cl</li> | ||
Latest revision as of 22:29, 27 October 2013
Gel Shift Assay
Gel Shift Assay
Reagents and Materials
- 1.3% agarose gel
- DNA of interest
- Purified protein sample
10x TALE binding 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
