Difference between revisions of "User:Paul Rothenberg/Notebook/Pauls Notebook/2013/02/25"

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(25 February 2013)
(25 February 2013)
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*1. Create a 1% agarose gel (1g agarose in 100 mL TAE) for gel electrophoresis
 
*1. Create a 1% agarose gel (1g agarose in 100 mL TAE) for gel electrophoresis
 +
*2. Run a DNA sample to test for expression
  
  
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*4. The TAE and agarose was poured into the electrophoresis chamber and left to harden; electrophoresis buffer was added following
 
*4. The TAE and agarose was poured into the electrophoresis chamber and left to harden; electrophoresis buffer was added following
 
*5. 5 microliters of DNA and 1 microliter of dye; 6 microliters of the DNA ladder were added to the wells
 
*5. 5 microliters of DNA and 1 microliter of dye; 6 microliters of the DNA ladder were added to the wells
 +
*6. The gel was run for  minutes at 90V
  
  

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25 February 2013

  • Objectives:
  • 1. Create a 1% agarose gel (1g agarose in 100 mL TAE) for gel electrophoresis
  • 2. Run a DNA sample to test for expression


  • Data:
  • 1. 50x TAE stock buffer was diluted to 1x TAE buffer, using 2 mL of 50x buffer and 98 mL of ultra-pure water (1)
  • 2. 0.25 grams of agarose was dissolved in 25 mL of TAE
  • 3. The TAE was microwaved for 45 seconds to dissolve the agarose
  • 4. The TAE and agarose was poured into the electrophoresis chamber and left to harden; electrophoresis buffer was added following
  • 5. 5 microliters of DNA and 1 microliter of dye; 6 microliters of the DNA ladder were added to the wells
  • 6. The gel was run for minutes at 90V