Performing Drosophila Crosses

Revision as of 18:00, 19 June 2013 by IsabelleHatfield (Talk | contribs)

Revision as of 18:00, 19 June 2013 by IsabelleHatfield (Talk | contribs)

  • Collect virgin females with appropriate marker and put into a new vial.
  • Store the vials from which virgins are collected at 18° C when not using.
  • Store vials from which males are collected at room temperature.
  • Once 10 virgin females from a strain have been collected, add 4 males with the appropriate marker from a different strain.
  • Label the vial to indicate the cross type and generation (A1 = the first generation of the first cross).
  • Store the crosses in an incubator.
  • After 5 days, flip the 14 flies into a new vial (there should be eggs visible at the surface of the food).
  • Label the vial appropriately (A2 = the second generation of the first cross).
  • Repeat this cycle until enough progeny from the crosses have been produced or until there are no parent males left.
  • The progeny will start eclosing after ~10 days.
  • Record the date that the flies begin eclosing.
  • Once there are at least 20 flies in the vial, collect the progeny and sort according to phenotype.
  • Record the number of flies of each phenotype born.
  • Place the males and females into separate vials.
  • There should be 5 - 15 progeny flies in each vial.
    • If necessary, separate/combine phenotypes to have an appropriate number of flies in the vial.
  • Label the vial with:
  1. Cross type/generation
  2. gender
  3. number of flies
  4. phenotype
  5. date born
  6. date added to vial.
  • Keep the progeny vials in an incubator.
  • Repeat this process during the six days following the date of first eclosure
    • Wait to sort until there are at least 20 flies in the vial (usually 2 to 3 times per vial)
  • After six days, toss the vial
  • Flip all progeny vials twice a week