BISC219/F11: Lab 2 Mutant Hunt: Difference between revisions

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#Scan the “mutagenized” worms on this plate and determine their phenotype.  Make sure you write this down.
#Scan the “mutagenized” worms on this plate and determine their phenotype.  Make sure you write this down.
#Transfer 1 putative mutant hermaphrodite to each of two new plates.  Take care not to transfer any other animals or eggs other than your putative mutant.<br>
#Transfer 1 putative mutant hermaphrodite to each of two new plates.  Take care not to transfer any other animals or eggs other than your putative mutant.<br>
#Label these 3 identical plates with the hermaphrodite mutant's strain information and your group's information (team color, initials, lab day, date). Use your <font color= blue><b>BLUE </b></font color> Sharpie for labeling these linkage analysis plates.  Labels belong on the side of the plate with the media in it or on the bottom of the plate with media in it - around the edge.  Tape makes it hard to see the worms on later days.  '''DO NOT write on the lids''' - they fall off and you will not know what cover goes to what bottom!
#Label these 2 identical plates with the hermaphrodite mutant's strain information and your group's information (team color, initials, lab day, date). Use your <font color= blue><b>BLUE </b></font color> Sharpie for labeling these linkage analysis plates.  Labels belong on the side of the plate with the media in it or on the bottom of the plate with media in it - around the edge.  Tape makes it hard to see the worms on later days.  '''DO NOT write on the lids''' - they fall off and you will not know what cover goes to what bottom!
#Put an elastic around the two linkage determination plates. Place them in your group's plastic box (make sure your box is labeled with your names and lab section on a piece of your team color tape).  
#Put an elastic around the two linkage determination plates. Place them in your group's plastic box (make sure your box is labeled with your names and lab section on a piece of your team color tape).  
#Place your box on the shelf in the incubator for your lab section.<br>
#Place your box on the shelf in the incubator for your lab section.<br>
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<br>
<br>
'''3 Days After Lab'''<br>
'''3 Days After Lab'''<br>
#Examine your three plates containing your mutant worms from the mutant hunt and their F1 progeny.  Are all the worms on at least one plate of the Dpy phenotype?  If '''YES''', then you are good to go on with the next cross. If you don't have all dumpy mutants in the F1 generation on a plate, you should '''not''' use that plate to select worms for the next cross. If neither of your plates contains all dumpy mutants, email your instructor ASAP!<br>
#Examine your two plates containing your mutant worms from the mutant hunt and their F1 progeny.  Are all the worms on at least one plate of the Dpy phenotype?  If '''YES''', then you are good to go on with the next cross. If you don't have all dumpy mutants in the F1 generation on a plate, you should '''not''' use that plate to select worms for the next cross. If neither of your plates contains all dumpy mutants, email your instructor ASAP!<br>
# If you have an appropriate plate for continuing: Set up a pair of replicate crosses between 4  Dpy L4 hermaphrodites (should still have the vulval clearing about 1/2 way down the body of the worm) and 3-4 wild type male worms. You will have to search to find the N2 male worms among the hermaphrodites in the wild type worm plates provided in your lab day's box at the back of the room. When you are finished, you should have two identical mating plates with 3-4 L4 hermaphrodites and 3-4 wild type males.<br>
# If you have an appropriate plate for continuing: Set up a pair of replicate crosses between 4  Dpy L4 hermaphrodites (should still have the vulval clearing about 1/2 way down the body of the worm) and 3-4 wild type male worms. You will have to search to find the N2 male worms among the hermaphrodites in the wild type worm plates provided in your lab day's box at the back of the room. When you are finished, you should have two identical mating plates with 3-4 L4 hermaphrodites and 3-4 wild type males.<br>
#Label these identical plates with the hermaphrodite mutant's strain information and your group's information including the date. Use your <font color= blue><b>BLUE </b></font color> Sharpie for labeling these linkage analysis/mapping plates. <br>
#Label these identical plates with the hermaphrodite mutant's strain information and your group's information including the date. Use your <font color= blue><b>BLUE </b></font color> Sharpie for labeling these linkage analysis/mapping plates. <br>

Latest revision as of 09:47, 16 September 2011

Lab 2: Start Forward Genetics Project: Testing a Mutant for True Breeding

To Do Today (per group)

  1. Choose one of the six plates of "mutagenized" worms at the front of the room
  2. Scan the “mutagenized” worms on this plate and determine their phenotype. Make sure you write this down.
  3. Transfer 1 putative mutant hermaphrodite to each of two new plates. Take care not to transfer any other animals or eggs other than your putative mutant.
  4. Label these 2 identical plates with the hermaphrodite mutant's strain information and your group's information (team color, initials, lab day, date). Use your BLUE Sharpie for labeling these linkage analysis plates. Labels belong on the side of the plate with the media in it or on the bottom of the plate with media in it - around the edge. Tape makes it hard to see the worms on later days. DO NOT write on the lids - they fall off and you will not know what cover goes to what bottom!
  5. Put an elastic around the two linkage determination plates. Place them in your group's plastic box (make sure your box is labeled with your names and lab section on a piece of your team color tape).
  6. Place your box on the shelf in the incubator for your lab section.
  7. Incubate your worms at 23°C for 3 days.


3 Days After Lab

  1. Examine your two plates containing your mutant worms from the mutant hunt and their F1 progeny. Are all the worms on at least one plate of the Dpy phenotype? If YES, then you are good to go on with the next cross. If you don't have all dumpy mutants in the F1 generation on a plate, you should not use that plate to select worms for the next cross. If neither of your plates contains all dumpy mutants, email your instructor ASAP!
  2. If you have an appropriate plate for continuing: Set up a pair of replicate crosses between 4 Dpy L4 hermaphrodites (should still have the vulval clearing about 1/2 way down the body of the worm) and 3-4 wild type male worms. You will have to search to find the N2 male worms among the hermaphrodites in the wild type worm plates provided in your lab day's box at the back of the room. When you are finished, you should have two identical mating plates with 3-4 L4 hermaphrodites and 3-4 wild type males.
  3. Label these identical plates with the hermaphrodite mutant's strain information and your group's information including the date. Use your BLUE Sharpie for labeling these linkage analysis/mapping plates.
  4. Incubate your worms at 23°C until next lab period.

Assignment

Remember to check the Assignment section of the wiki for instructions about the graded assignment due in the next lab and check the Weekly Calendar for other work to accomplish before the next lab.