Haynes Lab:Notebook/Lab Traning - Pradyumna Kadambi/2013/06/28: Difference between revisions

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(Autocreate 2013/06/28 Entry for Haynes_Lab:Notebook/Lab_Traning_-_Pradyumna_Kadambi)
 
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==Entry title==
==DH5α Incubation in Liquid Media 6/28/2013==
* Insert content here...
#With a pipetter, 3mL of LB+amp was added to a test tube.
#A colony was selected on the culture plate(plate was overgrown), and a circle was drawn where the colony was selected.
#Micropipette tip was lightly touched to the colony making sure not to scrape any of the agar gel. Micropipette tip was then ejected into test tube.
#Test tube was incubated with shaker for 7 hours at 37 degrees.


==DH5α Mini Prep with KAH013 6/28/2013==
*Colonies that Rene had incubated in liquid media on 6/27 were used.
#Using a micropipette, a 2mL centrifuge tube was filled with the incubated liquid media.
#The solution was centrifuged at 13.1g for 3 minutes (If a pellet has not completely condensed centrifuge again until pellet does condense).
#Using a micropipette, the supernatant was removed until 600μL of solution remained in the centrifuge tube. (Discard supernatant into the bleach container in the fume hood)
#Pellet was broken up using the vortex.
#Added 100μL of lysis buffer to the centrifuge tube and inverted 4-6 times and waited 1 min.
#Added 350μL of lysis buffer. Invert the solution until it turns yellow, make sure no blue pockets are left.
#Centrifuge the solution at
#
#
#
'''


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Revision as of 20:53, 30 June 2013

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DH5α Incubation in Liquid Media 6/28/2013

  1. With a pipetter, 3mL of LB+amp was added to a test tube.
  2. A colony was selected on the culture plate(plate was overgrown), and a circle was drawn where the colony was selected.
  3. Micropipette tip was lightly touched to the colony making sure not to scrape any of the agar gel. Micropipette tip was then ejected into test tube.
  4. Test tube was incubated with shaker for 7 hours at 37 degrees.

DH5α Mini Prep with KAH013 6/28/2013

  • Colonies that Rene had incubated in liquid media on 6/27 were used.
  1. Using a micropipette, a 2mL centrifuge tube was filled with the incubated liquid media.
  2. The solution was centrifuged at 13.1g for 3 minutes (If a pellet has not completely condensed centrifuge again until pellet does condense).
  3. Using a micropipette, the supernatant was removed until 600μL of solution remained in the centrifuge tube. (Discard supernatant into the bleach container in the fume hood)
  4. Pellet was broken up using the vortex.
  5. Added 100μL of lysis buffer to the centrifuge tube and inverted 4-6 times and waited 1 min.
  6. Added 350μL of lysis buffer. Invert the solution until it turns yellow, make sure no blue pockets are left.
  7. Centrifuge the solution at


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