Tossinggloves andtubes intothe sharpsdisposalStillbriningdrinks intothe labNofigurelegendsUsing directisolation foreverymethod topicCopy andpastepsychopathUsing theP20 tipswith P200pipetteTurning dialto 005instead of050 for 5 uLusing a P10Gettingcontaminationon spot plateand plaqueassayKeepreferencingDirectIsolationProtocol 5.3 CUsingP200instead ofP20Going up to 3 mLon serologicalpipette but usingthe wrong side tomeasureNotrecognizingyou hadphages on aspot test plateCould notlight abunsenburnerPushedtoo hardon syringewith filterUsing bacteriaandbacteriophageinterchangeablyUseddiameter tocalculatearea insteadof radiusLeft pipettepump rubberholder onpipetteSending labreports forme to lookat, at 12 AMPushing plungerto second stopon micro-pipettor whendrawing upliquidUsing a 10mLserologicalpipette for 1mLNotsayingthat H isfor HopeyTurned overplateimmediateafter addingtop agarAccidentallythrowing awayimportanttubes orsamplesTaking apicture ofyour spot testplate withtape still onPoured topagar onplate coverinstead100% plaqueassaysuccess rateDid not put filteron syringe forenrichedisolationmixtureNOTE-TAKING!Labelingthe top ofthe plateTried to lightbunsenburner withgas turnedoffOnesentence ofbackgroundinformationNotspreadingthe top agarevenly onthe plateLeft top agarout too longand it solidifiedbefore pouring100101102Forgettingto take apicture ofyour plateHanded ina labreport lateDropped apipette tipinto tube fullof liquidForgettinglab coatsPouring thehost bacteriaonto a platewithout addingtop agarTossinggloves andtubes intothe sharpsdisposalStillbriningdrinks intothe labNofigurelegendsUsing directisolation foreverymethod topicCopy andpastepsychopathUsing theP20 tipswith P200pipetteTurning dialto 005instead of050 for 5 uLusing a P10Gettingcontaminationon spot plateand plaqueassayKeepreferencingDirectIsolationProtocol 5.3 CUsingP200instead ofP20Going up to 3 mLon serologicalpipette but usingthe wrong side tomeasureNotrecognizingyou hadphages on aspot test plateCould notlight abunsenburnerPushedtoo hardon syringewith filterUsing bacteriaandbacteriophageinterchangeablyUseddiameter tocalculatearea insteadof radiusLeft pipettepump rubberholder onpipetteSending labreports forme to lookat, at 12 AMPushing plungerto second stopon micro-pipettor whendrawing upliquidUsing a 10mLserologicalpipette for 1mLNotsayingthat H isfor HopeyTurned overplateimmediateafter addingtop agarAccidentallythrowing awayimportanttubes orsamplesTaking apicture ofyour spot testplate withtape still onPoured topagar onplate coverinstead100% plaqueassaysuccess rateDid not put filteron syringe forenrichedisolationmixtureNOTE-TAKING!Labelingthe top ofthe plateTried to lightbunsenburner withgas turnedoffOnesentence ofbackgroundinformationNotspreadingthe top agarevenly onthe plateLeft top agarout too longand it solidifiedbefore pouring100101102Forgettingto take apicture ofyour plateHanded ina labreport lateDropped apipette tipinto tube fullof liquidForgettinglab coatsPouring thehost bacteriaonto a platewithout addingtop agar

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