Handed ina labreport lateLeft pipettepump rubberholder onpipetteCopy andpastepsychopathGettingcontaminationon spot plateand plaqueassayStillbriningdrinks intothe labTossinggloves andtubes intothe sharpsdisposalUseddiameter tocalculatearea insteadof radiusNotsayingthat H isfor HopeyUsing directisolation foreverymethod topicTurned overplateimmediateafter addingtop agarPouring thehost bacteriaonto a platewithout addingtop agarNofigurelegendsUsing bacteriaandbacteriophageinterchangeablyUsingP200instead ofP20Sending labreports forme to lookat, at 12 AMPoured topagar onplate coverinstead100% plaqueassaysuccess rateGoing up to 3 mLon serologicalpipette but usingthe wrong side tomeasureTaking apicture ofyour spot testplate withtape still onForgettinglab coatsPushedtoo hardon syringewith filterOnesentence ofbackgroundinformation100101102Tried to lightbunsenburner withgas turnedoffUsing theP20 tipswith P200pipetteKeepreferencingDirectIsolationProtocol 5.3 CNotspreadingthe top agarevenly onthe plateLeft top agarout too longand it solidifiedbefore pouringNOTE-TAKING!Forgettingto take apicture ofyour plateNotrecognizingyou hadphages on aspot test platePushing plungerto second stopon micro-pipettor whendrawing upliquidTurning dialto 005instead of050 for 5 uLusing a P10Did not put filteron syringe forenrichedisolationmixtureAccidentallythrowing awayimportanttubes orsamplesCould notlight abunsenburnerUsing a 10mLserologicalpipette for 1mLLabelingthe top ofthe plateDropped apipette tipinto tube fullof liquidHanded ina labreport lateLeft pipettepump rubberholder onpipetteCopy andpastepsychopathGettingcontaminationon spot plateand plaqueassayStillbriningdrinks intothe labTossinggloves andtubes intothe sharpsdisposalUseddiameter tocalculatearea insteadof radiusNotsayingthat H isfor HopeyUsing directisolation foreverymethod topicTurned overplateimmediateafter addingtop agarPouring thehost bacteriaonto a platewithout addingtop agarNofigurelegendsUsing bacteriaandbacteriophageinterchangeablyUsingP200instead ofP20Sending labreports forme to lookat, at 12 AMPoured topagar onplate coverinstead100% plaqueassaysuccess rateGoing up to 3 mLon serologicalpipette but usingthe wrong side tomeasureTaking apicture ofyour spot testplate withtape still onForgettinglab coatsPushedtoo hardon syringewith filterOnesentence ofbackgroundinformation100101102Tried to lightbunsenburner withgas turnedoffUsing theP20 tipswith P200pipetteKeepreferencingDirectIsolationProtocol 5.3 CNotspreadingthe top agarevenly onthe plateLeft top agarout too longand it solidifiedbefore pouringNOTE-TAKING!Forgettingto take apicture ofyour plateNotrecognizingyou hadphages on aspot test platePushing plungerto second stopon micro-pipettor whendrawing upliquidTurning dialto 005instead of050 for 5 uLusing a P10Did not put filteron syringe forenrichedisolationmixtureAccidentallythrowing awayimportanttubes orsamplesCould notlight abunsenburnerUsing a 10mLserologicalpipette for 1mLLabelingthe top ofthe plateDropped apipette tipinto tube fullof liquid

BIO1027 Growing Pains - 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. Handed in a lab report late
  2. Left pipette pump rubber holder on pipette
  3. Copy and paste psychopath
  4. Getting contamination on spot plate and plaque assay
  5. Still brining drinks into the lab
  6. Tossing gloves and tubes into the sharps disposal
  7. Used diameter to calculate area instead of radius
  8. Not saying that H is for Hopey
  9. Using direct isolation for every method topic
  10. Turned over plate immediate after adding top agar
  11. Pouring the host bacteria onto a plate without adding top agar
  12. No figure legends
  13. Using bacteria and bacteriophage interchangeably
  14. Using P200 instead of P20
  15. Sending lab reports for me to look at, at 12 AM
  16. Poured top agar on plate cover instead
  17. 100% plaque assay success rate
  18. Going up to 3 mL on serological pipette but using the wrong side to measure
  19. Taking a picture of your spot test plate with tape still on
  20. Forgetting lab coats
  21. Pushed too hard on syringe with filter
  22. One sentence of background information
  23. 100 101 102
  24. Tried to light bunsen burner with gas turned off
  25. Using the P20 tips with P200 pipette
  26. Keep referencing Direct Isolation Protocol 5.3 C
  27. Not spreading the top agar evenly on the plate
  28. Left top agar out too long and it solidified before pouring
  29. NOTE-TAKING!
  30. Forgetting to take a picture of your plate
  31. Not recognizing you had phages on a spot test plate
  32. Pushing plunger to second stop on micro-pipettor when drawing up liquid
  33. Turning dial to 005 instead of 050 for 5 uL using a P10
  34. Did not put filter on syringe for enriched isolation mixture
  35. Accidentally throwing away important tubes or samples
  36. Could not light a bunsen burner
  37. Using a 10 mL serological pipette for 1 mL
  38. Labeling the top of the plate
  39. Dropped a pipette tip into tube full of liquid