Difference between revisions of "Haynes Lab:Notebook/Engineering PC-TFs/2012/11/08"

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|style="background-color: #EEE"|[[Image:owwnotebook_icon.png|128px]]<span style="font-size:22px;"> Engineering PC-TFs</span>
 
|style="background-color: #EEE"|[[Image:owwnotebook_icon.png|128px]]<span style="font-size:22px;"> Engineering PC-TFs</span>
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==Summary==
 
==Summary==
Assembly Check of PCR Reactions 1,2,3,4<i>
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<i>Assembly Check of PCR Reactions 1,2,3,4
  
 
* Gel Electrophoresis
 
* Gel Electrophoresis
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*Turn on electrophoresis and let run for thirty minutes.
 
*Turn on electrophoresis and let run for thirty minutes.
  
The assembly did not work. No bands were seen when placed under UV light.<b>
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<b>The assembly did not work. No bands were seen when placed under UV light.
  
  

Latest revision as of 22:14, 26 September 2017

Owwnotebook icon.png Engineering PC-TFs Report.pngMain project page
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Summary

Assembly Check of PCR Reactions 1,2,3,4

  • Gel Electrophoresis

Follow steps for gel electrophoresis.

  • Orient top notch of gel electrophoresis apparatus. Place gel tray into larger tray.
  • Create 1% gel by putting .6 grams of agarose into flask.
  • Microwave agarose solution for 30 seconds
  • Using hot gloves, grab flask out of microwave and swirl flask vigorously. Place back in microwave for 30 more seconds.
  • When flask is taken out of microwave, make sure that the agarose is completed dissolved.
  • Set up wells on gel electrophoresis apparatus. The mold for the first digest is B-10. Use the thin "teeth" and slip in the notches.
  • Add EtBr (ethidium bromide) to the agarose gel. There should be 1 microliter of EtBr per 10ml of agarose gel. Therefore, 6 µL.
  • Pour gel into tray. Wait twenty minutes for gel to settle.
  • Wash the agarose gel flask.
  • Pipette 15 μL of DNA ladder into first well. Pipette 5μL of PCR reactions into subsequent wells.
  • Turn on electrophoresis and let run for thirty minutes.

The assembly did not work. No bands were seen when placed under UV light.