Difference between revisions of "Team:UCL/Experiments"

 
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<a href="https://2015.igem.org/Team:UCL/Home"><li>Home</li></a>
 
<a href="https://2015.igem.org/Team:UCL/Description"><li>Project</li></a>   
 
<a href="https://2015.igem.org/Team:UCL/Parts"><li>Parts</li></a>   
 
<a href="https://2015.igem.org/Team:UCL/Experiments"><li>Experiments &amp; Protocols</li></a> 
 
 
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<a href="https://2015.igem.org/Team:UCL/Team"><li>Team</li></a>
 
<a href="https://2015.igem.org/Team:UCL/Interlabstudy"><li>InterLab Study</li></a>
 
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<h2>Experiments &amp; Protocols</h2>
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<div style="height:80px"></div>
 
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<p>Describe the experiments, research and protocols you used in your iGEM project.</p>
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<ul>
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<li> Protocols </li>
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<li> Experiments </li>
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<li>Documentation of the development of your project </li>
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</ul>
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<div id="transformation"><h4>Transformation protocol </h4>
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1. (If using part from the distribution: resuspend the DNA in 10 ul of MiliQ water, making sure that it turns red. Wait 10 minutes before adding the DNA to cells)<br/>
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2. Put a tube of NEB DH 5 alpha <i>E. coli</i> cells on ice and wait until they thaw completely. Divide the cells into 50 ul aliquotes. <br/>
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3. Add 1 ul of plasmid DNA to 50 ul of cells. <br/>
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4. Mix by carefully flicking the tube. Do not vortex or pipette in and out! <br/>
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5. Place the mixture on ice for 30 minutes. <br/>
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6. Heat shock the cells at 42 °C for 30 seconds and immediately put on back on ice.<br/>
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7. Keep cells on ice for next 5 minutes. Do not mix. <br/>
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8. Pipette 950 ul of SOC media kept at room temperature into the mixture. <br/>
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9. Incubate the mixture at 37 °C for 60 minutes <br/>
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10. Plate 50 ul of cells to the plate with appropriate antibiotic and incubate overnight at 37 °C
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<br/><br/>
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Latest revision as of 00:29, 6 August 2015