Team:INSA Toulouse/contenu/lab practice/notebook/protocols/integration

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Revision as of 11:52, 3 October 2013

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Notebook

Protocols

Integration Protocols

Transduction Protocol

  • Preparation of the phage (lisis of the donor strain)
    1. Dilution of an overnight culture at 1/100 in LB and CaCL2 5mM
    2. Incubation until DO=1
    3. Mix 0,3 mL of bacterias with 10^6 phages P1vir = 10-50µL
    4. Incubation at 37°c during 20 min
    5. Add 3mL of Soft Agar (50% hot LB + 50% LB agar) with the mix of bacterias then spread on LB agar plate
    6. Incubation one night at 30°C
    7. Swab of the phages and bacterias contained in the soft agar
  • Pipette 10uL of dH2O (distilled water) into the well. Pipette up and down a few times and let sit for 5 minutes to make sure the dried DNA is fully resuspended. We recommend that you do not use TE to resuspend the dried DNA.


* To know which antibiotics to use, look at the plasmid that the part is in. The naming scheme for plasmids is specifically designed to indicate antibiotic resistance.
Note: There is not enough DNA in each well to perform anything but transformations.

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