Haynes Lab:Notebook/Lab Traning - Pradyumna Kadambi/2013/07/26: Difference between revisions

From OpenWetWare
Jump to navigationJump to search
(Autocreate 2013/07/26 Entry for Haynes_Lab:Notebook/Lab_Traning_-_Pradyumna_Kadambi)
 
Line 6: Line 6:
| colspan="2"|
| colspan="2"|
<!-- ##### DO NOT edit above this line unless you know what you are doing. ##### -->
<!-- ##### DO NOT edit above this line unless you know what you are doing. ##### -->
==Entry title==
==Transformation of DH5α with KAH013 07/26/13==
* Insert content here...
#LB+amp plates were taken from fridge and placed in incubator at 37degrees.  
#KAH013 plasmid was taken from the fridge.
#In a 1mL tube, 9μL of dH2O and 1μL of KAH013 were added.
#DH5α cells were taken from the freezer and placed in an ice bath.
#Waited 10 mins for the DH5α cells to thaw.
#In the 1mL tube containing the dH2O and the plasmid, 50μL of DH5α was added.
#Waited 10 mins for the bacteria to accept the plasmid.
#Pipetted the 60μL contents of the 1mL tube onto the warmed LB-amp plates.
#Around 6-10 rolling beads were used to spread the bacteria.
#Plates were placed in incubator at 37degrees for 12 hours.
#Heather came in after 12 hours to remove the plates from the incubator.
 





Revision as of 14:56, 4 August 2013

Project name <html><img src="/images/9/94/Report.png" border="0" /></html> Main project page
<html><img src="/images/c/c3/Resultset_previous.png" border="0" /></html>Previous entry<html>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</html>Next entry<html><img src="/images/5/5c/Resultset_next.png" border="0" /></html>

Transformation of DH5α with KAH013 07/26/13

  1. LB+amp plates were taken from fridge and placed in incubator at 37degrees.
  2. KAH013 plasmid was taken from the fridge.
  3. In a 1mL tube, 9μL of dH2O and 1μL of KAH013 were added.
  4. DH5α cells were taken from the freezer and placed in an ice bath.
  5. Waited 10 mins for the DH5α cells to thaw.
  6. In the 1mL tube containing the dH2O and the plasmid, 50μL of DH5α was added.
  7. Waited 10 mins for the bacteria to accept the plasmid.
  8. Pipetted the 60μL contents of the 1mL tube onto the warmed LB-amp plates.
  9. Around 6-10 rolling beads were used to spread the bacteria.
  10. Plates were placed in incubator at 37degrees for 12 hours.
  11. Heather came in after 12 hours to remove the plates from the incubator.