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Colony PCR

Objective

Author(s): Ada Jiang

Screen bacterial colonies for presence of desired DNA construct by directly using cell lysate for PCR amplification.

Procedure

  1. Prepare template material. There are several options:
    1. Pick a colony (ideally fresh) and mix directly in PCR reaction mixture (will look slightly cloudy, don’t pick up too much cell material)
    2. Option A but replace water content in PCR mix with TE buffer.
    3. Pick a colony and dissolve in 50-100 uL media / DMSO / water. Use 1 µL of the cell lysate for PCR.
    4. Use 1 uL of fresh overnight cultu
  2. Run PCR cycle, using Polymerase Chain Reaction (PCR) with NEB Q5 High-Fidelity 2X Master Mix.
    1. Consider setting a longer initial denature step to help break up the cells.