Could notlight abunsenburnerGettingcontaminationon spot plateand plaqueassayPushing plungerto second stopon micro-pipettor whendrawing upliquidPushedtoo hardon syringewith filterDropped apipette tipinto tube fullof liquidOnesentence ofbackgroundinformation100% plaqueassaysuccess rateAccidentallythrowing awayimportanttubes orsamplesDid not put filteron syringe forenrichedisolationmixtureTaking apicture ofyour spot testplate withtape still onTurned overplateimmediateafter addingtop agarUsingP200instead ofP20Sending labreports forme to lookat, at 12 AMNotrecognizingyou hadphages on aspot test plateLeft top agarout too longand it solidifiedbefore pouringUseddiameter tocalculatearea insteadof radiusNOTE-TAKING!Using bacteriaandbacteriophageinterchangeablyGoing up to 3 mLon serologicalpipette but usingthe wrong side tomeasureForgettingto take apicture ofyour plateNotspreadingthe top agarevenly onthe plateCopy andpastepsychopathNotsayingthat H isfor HopeyForgettinglab coatsTried to lightbunsenburner withgas turnedoffTurning dialto 005instead of050 for 5 uLusing a P10Using a 10mLserologicalpipette for 1mLLeft pipettepump rubberholder onpipetteHanded ina labreport lateUsing directisolation foreverymethod topicTossinggloves andtubes intothe sharpsdisposalLabelingthe top ofthe platePouring thehost bacteriaonto a platewithout addingtop agarKeepreferencingDirectIsolationProtocol 5.3 C100101102NofigurelegendsStillbriningdrinks intothe labUsing theP20 tipswith P200pipettePoured topagar onplate coverinsteadCould notlight abunsenburnerGettingcontaminationon spot plateand plaqueassayPushing plungerto second stopon micro-pipettor whendrawing upliquidPushedtoo hardon syringewith filterDropped apipette tipinto tube fullof liquidOnesentence ofbackgroundinformation100% plaqueassaysuccess rateAccidentallythrowing awayimportanttubes orsamplesDid not put filteron syringe forenrichedisolationmixtureTaking apicture ofyour spot testplate withtape still onTurned overplateimmediateafter addingtop agarUsingP200instead ofP20Sending labreports forme to lookat, at 12 AMNotrecognizingyou hadphages on aspot test plateLeft top agarout too longand it solidifiedbefore pouringUseddiameter tocalculatearea insteadof radiusNOTE-TAKING!Using bacteriaandbacteriophageinterchangeablyGoing up to 3 mLon serologicalpipette but usingthe wrong side tomeasureForgettingto take apicture ofyour plateNotspreadingthe top agarevenly onthe plateCopy andpastepsychopathNotsayingthat H isfor HopeyForgettinglab coatsTried to lightbunsenburner withgas turnedoffTurning dialto 005instead of050 for 5 uLusing a P10Using a 10mLserologicalpipette for 1mLLeft pipettepump rubberholder onpipetteHanded ina labreport lateUsing directisolation foreverymethod topicTossinggloves andtubes intothe sharpsdisposalLabelingthe top ofthe platePouring thehost bacteriaonto a platewithout addingtop agarKeepreferencingDirectIsolationProtocol 5.3 C100101102NofigurelegendsStillbriningdrinks intothe labUsing theP20 tipswith P200pipettePoured topagar onplate coverinstead

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