Difference between revisions of "IGEM:Peking/2007/Count:Conjugation"

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(New page: ==Conjugation Test== *choose the Donor cell and Recipient Cell which must be different Antibiotic. '''*Day1:''' #Get the plates from -4 fridge:C600-R751_psc101(Tc+), Dh5α_psb1A2(Amp+),...)
 
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==Conjugation Test==
+
=Conjugation Test=
 
*choose the Donor cell and Recipient Cell which must be different Antibiotic.
 
*choose the Donor cell and Recipient Cell which must be different Antibiotic.
  
'''*Day1:'''
+
==*Day1:==
#Get the plates from -4 fridge:C600-R751_psc101(Tc+), Dh5α_psb1A2(Amp+), C600_R751, Dh5α_psc101
+
#Get the plates from -4 fridge:Donor, Recipient, Control.
 
#Amplification Culture in liquid LB for 12 hours.
 
#Amplification Culture in liquid LB for 12 hours.
'''*day 2:'''
+
 
 +
==*day 2:==
 
#put 2mL of culture into 20mL of LB with antibiotics, sub-culturing.
 
#put 2mL of culture into 20mL of LB with antibiotics, sub-culturing.
 +
 
===Donor===
 
===Donor===
 
#Test OD600 after 30minutes of sub-culturing, stop subculturing when OD600 reached 0.45~0.6(log phase).
 
#Test OD600 after 30minutes of sub-culturing, stop subculturing when OD600 reached 0.45~0.6(log phase).
 
#After sub-culturing decant the 500uL culture into a 1.5mL tube.
 
#After sub-culturing decant the 500uL culture into a 1.5mL tube.
#spin down (top speed for 1 min.), discard fluid.
+
#spin down (top speed for 1 min), discard fluid.
 
#resuspend in 500mL LB(NO Antibiotic!), vortex.
 
#resuspend in 500mL LB(NO Antibiotic!), vortex.
 
#Repeat steps 3-4-3 in this order then progress to step 6.
 
#Repeat steps 3-4-3 in this order then progress to step 6.
 
#Re-suspend with 500mL LB.
 
#Re-suspend with 500mL LB.
 
#Place the cell suspension on ice.
 
#Place the cell suspension on ice.
 +
 
===Recipient===
 
===Recipient===
 
#decant the recipient cells(500uL culture into a 1.5mL tube) when reached the stationary phase.
 
#decant the recipient cells(500uL culture into a 1.5mL tube) when reached the stationary phase.
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===Plating the conjugant mix ===
 
===Plating the conjugant mix ===
  
===result===
+
==see also==
 +
[[UC Berkeley/2006/Conjugation]]

Revision as of 02:39, 11 August 2007

Conjugation Test

  • choose the Donor cell and Recipient Cell which must be different Antibiotic.

*Day1:

  1. Get the plates from -4 fridge:Donor, Recipient, Control.
  2. Amplification Culture in liquid LB for 12 hours.

*day 2:

  1. put 2mL of culture into 20mL of LB with antibiotics, sub-culturing.

Donor

  1. Test OD600 after 30minutes of sub-culturing, stop subculturing when OD600 reached 0.45~0.6(log phase).
  2. After sub-culturing decant the 500uL culture into a 1.5mL tube.
  3. spin down (top speed for 1 min), discard fluid.
  4. resuspend in 500mL LB(NO Antibiotic!), vortex.
  5. Repeat steps 3-4-3 in this order then progress to step 6.
  6. Re-suspend with 500mL LB.
  7. Place the cell suspension on ice.

Recipient

  1. decant the recipient cells(500uL culture into a 1.5mL tube) when reached the stationary phase.
  2. spin down (top speed for 1 min.), discard fluid.
  3. resuspend in 500mL LB(NO Antibiotic!), vortex.
  4. Repeat steps 3-4-3 in this order then progress to step 6.
  5. Re-suspend with 500mL LB.
  6. Place the cell suspension on ice.

Plating the conjugant mix

see also

UC Berkeley/2006/Conjugation