BISC219/F12: Lab 2 Mutant Hunt: Difference between revisions

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#Incubate your worms at 23°C until next lab period.
#Incubate your worms at 23°C until next lab period.


<math>Insert formula here</math>== Assignment ==
== Assignment ==
Remember to check the [http://www.openwetware.org/wiki/BISC219/F12:Assignments 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. [http://www.openwetware.org/wiki/BISC219/F12:_Assignment_Series2_Outline_Summary Homework Lab 2 link]
Remember to check the [http://openwetware.org/wiki/BISC219/F12:_Assignment_Series2_Outline_Summary | Assignment Series 2 Outline/Summary & Linkage Analysis Explanation] of the wiki for instructions about the graded assignment due in the next lab and check the Weekly Lab Planner section of the  [[BISC219/F12:Calendars/Planner| Weekly Calendar]] for other work to accomplish before the next lab.  
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[[BISC219/F12: Lab 7  | Lab 7: Complete Mapping: Score]]<br>
[[BISC219/F12: Lab 7  | Lab 7: Complete Mapping: Score]]<br>
'''Series3:'''<BR>
'''Series3:'''<BR>
[[BISC219/F12:RNA interference | RNA interference]]<BR>
[[BISC219/F12: RNAi General Information| Background Information on Project 3: Investigating Gene Regulation Using RNAi]] <br>
[[BISC219/F12: RNAi General Information | RNAi General Information]] <br>
[[BISC219/F12: Media Recipes | Media Recipes]]<br>
[[BISC219/F12: Media Recipes | Media Recipes]]<br>
[[BISC219/F12: RNAi Lab 5 | Lab 5: Picking your gene to RNAi]]<br>
[[BISC219/F12: RNAi Lab 7 | Lab 7: Identifying a bacterial colony containing our plasmid of interest  ]]<br>
[[BISC219/F12: RNAi Lab 6 | Lab 6: Cloning your gene of interest]]<br>
[[BISC219/F12: RNAi Lab 8 | Lab 8: Creating the feeding strain of bacteria for RNAi]]<br>
[[BISC219/F12: RNAi Lab 7  | Lab 7: Picking your transformant]]<br>
[[BISC219/F12: RNAi Lab 9 | Lab 9: Induction of feeding strain to produce dsRNA and feeding worms]]<br>
[[BISC219/F12: RNAi Lab 8 | Lab 8: Plasmid purification and transformation]]<br>
[[BISC219/F12: RNAi Lab 10 | Lab 10: Phenotypic analysis of treated vs untreated worms]]<br>
[[BISC219/F12: RNAi Lab | Lab 9: Induction of bacteria for RNAi]]<br>
[[BISC219/F12: RNAi Lab 11 | Lab 11: Writing Workshop]]<br>
[[BISC219/F12: RNAi Lab 10 | Lab 10: Scoring your worms]]<br>
[[BISC219/F12: RNAi Lab 12 | Lab 12: Writing Conferences]]<br>
[[BISC219/F12: RNAi Lab 11 | Lab 11: ]]<br><br>
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Latest revision as of 09:04, 28 August 2012

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. 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 phenotype 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 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 wild type 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 Series 2 Outline/Summary & Linkage Analysis Explanation of the wiki for instructions about the graded assignment due in the next lab and check the Weekly Lab Planner section of the Weekly Calendar for other work to accomplish before the next lab.