Team:Washington/Protocols/Transformation

From 2011.igem.org

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=General Transformation Protocol=
=General Transformation Protocol=
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#Thaw 25 - 200 μl TB buffer cells on ice.  Do not use glass tubes, which adsorb DNA.
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#Thaw 20 μl CCMB buffer cells on ice.  Do not use glass tubes, which adsorb DNA.
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#Add DNA, pipette gently to mix (keep volume of DNA less than 5% of the cell volume)
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#Add 20 μl DNA, pipette gently to mix (keep volume of DNA less than 5% of the cell volume)
#Incubate on ice for 30 minutes
#Incubate on ice for 30 minutes
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#*Note: If you are in a rush, you can shorten this incubation time to 5-10 min.
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:Note: If you are in a rush, you can shorten this incubation time to 5-10 min.
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#Incubate cells for 30 seconds at 42°C.
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#Incubate cells for 30-90 (1 min) seconds at 42°C.
#Incubate cells on ice for 2 min.
#Incubate cells on ice for 2 min.
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#Add 4 volumes of room temperature [[SOC]] (not critical)
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#Add 200mL of room temperature TB.
#Incubate for 1 hour at 37°C on shaker.
#Incubate for 1 hour at 37°C on shaker.
#*Note: Can also save some time here by reducing incubation to ~45 min.
#*Note: Can also save some time here by reducing incubation to ~45 min.

Revision as of 01:41, 14 September 2011


General Transformation Protocol

  1. Thaw 20 μl CCMB buffer cells on ice. Do not use glass tubes, which adsorb DNA.
  2. Add 20 μl DNA, pipette gently to mix (keep volume of DNA less than 5% of the cell volume)
  3. Incubate on ice for 30 minutes
Note: If you are in a rush, you can shorten this incubation time to 5-10 min.
  1. Incubate cells for 30-90 (1 min) seconds at 42°C.
  2. Incubate cells on ice for 2 min.
  3. Add 200mL of room temperature TB.
  4. Incubate for 1 hour at 37°C on shaker.
    • Note: Can also save some time here by reducing incubation to ~45 min.
    • Note: Step can be eliminated if plating on Amp plates, but not most other antibiotics
  5. Spread 100-300 μl onto a plate made with appropriate antibiotic.
  6. Grow overnight at 37°C.


Adapted from OpenWetWare protocol.