M1V1=M2V2for all damageand controlvolumes arepresentTableheading inbold at thetop of tableBe specificabout amountconcentrationsof stainsPurpose -Described inown wordswithrationalespecificname ofculture(0.5mMH2O2)Conclusion-washypothesisconfirmedAre pastproceduresincluded thatcontribute tothis lab?Allcolors/symbolsare defined infigure legendResults -focus on thewhy(scientificgoal)consistentcolor andline type foreach culturetable with cellculture, yeastculture, damage,YPD, and total(should reflectcalculations)FutureworksectionincludedWhatdoes ourdata tellusResults -ClearlystatedhypothesisIs theprocedure inyou're ownwords with alldetailsincluded?Title - notjust"assay 1"Is theprocedurein pasttense?x-axis is timeelapsedinstead ofdiscrete timepointsHow didyou testyourhypothesisNameandDateY-axis is# ofcells/mLfigure titlesummarizesthe mainresultsGrowth datatable withOD600 for eachcell damageand when itwas recordedconcludewhat youlearnedfrom assayM1V1=M2V2for all damageand controlvolumes arepresentTableheading inbold at thetop of tableBe specificabout amountconcentrationsof stainsPurpose -Described inown wordswithrationalespecificname ofculture(0.5mMH2O2)Conclusion-washypothesisconfirmedAre pastproceduresincluded thatcontribute tothis lab?Allcolors/symbolsare defined infigure legendResults -focus on thewhy(scientificgoal)consistentcolor andline type foreach culturetable with cellculture, yeastculture, damage,YPD, and total(should reflectcalculations)FutureworksectionincludedWhatdoes ourdata tellusResults -ClearlystatedhypothesisIs theprocedure inyou're ownwords with alldetailsincluded?Title - notjust"assay 1"Is theprocedurein pasttense?x-axis is timeelapsedinstead ofdiscrete timepointsHow didyou testyourhypothesisNameandDateY-axis is# ofcells/mLfigure titlesummarizesthe mainresultsGrowth datatable withOD600 for eachcell damageand when itwas recordedconcludewhat youlearnedfrom assay

Untitled Bingo - Call List

(Print) Use this randomly generated list as your call list when playing the game. There is no need to say the BINGO column name. Place some kind of mark (like an X, a checkmark, a dot, tally mark, etc) on each cell as you announce it, to keep track. You can also cut out each item, place them in a bag and pull words from the bag.


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  1. M1V1=M2V2 for all damage and control volumes are present
  2. Table heading in bold at the top of table
  3. Be specific about amount concentrations of stains
  4. Purpose - Described in own words with rationale
  5. specific name of culture (0.5mM H2O2)
  6. Conclusion-was hypothesis confirmed
  7. Are past procedures included that contribute to this lab?
  8. All colors/symbols are defined in figure legend
  9. Results - focus on the why (scientific goal)
  10. consistent color and line type for each culture
  11. table with cell culture, yeast culture, damage, YPD, and total (should reflect calculations)
  12. Future work section included
  13. What does our data tell us
  14. Results - Clearly stated hypothesis
  15. Is the procedure in you're own words with all details included?
  16. Title - not just "assay 1"
  17. Is the procedure in past tense?
  18. x-axis is time elapsed instead of discrete time points
  19. How did you test your hypothesis
  20. Name and Date
  21. Y-axis is # of cells/mL
  22. figure title summarizes the main results
  23. Growth data table with OD600 for each cell damage and when it was recorded
  24. conclude what you learned from assay