Stillbriningdrinks intothe labHanded ina labreport lateGoing up to 3 mLon serologicalpipette but usingthe wrong side tomeasureDropped apipette tipinto tube fullof liquid100101102Could notlight abunsenburnerUseddiameter tocalculatearea insteadof radiusSending labreports forme to lookat, at 12 AMTaking apicture ofyour spot testplate withtape still onPushedtoo hardon syringewith filterForgettingto take apicture ofyour plateLeft top agarout too longand it solidifiedbefore pouringForgettinglab coatsNotrecognizingyou hadphages on aspot test plate100% plaqueassaysuccess rateUsing bacteriaandbacteriophageinterchangeablyUsing a 10mLserologicalpipette for 1mLUsingP200instead ofP20Notsayingthat H isfor HopeyUsing directisolation foreverymethod topicGettingcontaminationon spot plateand plaqueassayKeepreferencingDirectIsolationProtocol 5.3 CPoured topagar onplate coverinsteadCopy andpastepsychopathUsing theP20 tipswith P200pipettePushing plungerto second stopon micro-pipettor whendrawing upliquidTurned overplateimmediateafter addingtop agarNOTE-TAKING!Tried to lightbunsenburner withgas turnedoffAccidentallythrowing awayimportanttubes orsamplesNofigurelegendsOnesentence ofbackgroundinformationDid not put filteron syringe forenrichedisolationmixtureTossinggloves andtubes intothe sharpsdisposalTurning dialto 005instead of050 for 5 uLusing a P10Labelingthe top ofthe plateLeft pipettepump rubberholder onpipetteNotspreadingthe top agarevenly onthe platePouring thehost bacteriaonto a platewithout addingtop agarStillbriningdrinks intothe labHanded ina labreport lateGoing up to 3 mLon serologicalpipette but usingthe wrong side tomeasureDropped apipette tipinto tube fullof liquid100101102Could notlight abunsenburnerUseddiameter tocalculatearea insteadof radiusSending labreports forme to lookat, at 12 AMTaking apicture ofyour spot testplate withtape still onPushedtoo hardon syringewith filterForgettingto take apicture ofyour plateLeft top agarout too longand it solidifiedbefore pouringForgettinglab coatsNotrecognizingyou hadphages on aspot test plate100% plaqueassaysuccess rateUsing bacteriaandbacteriophageinterchangeablyUsing a 10mLserologicalpipette for 1mLUsingP200instead ofP20Notsayingthat H isfor HopeyUsing directisolation foreverymethod topicGettingcontaminationon spot plateand plaqueassayKeepreferencingDirectIsolationProtocol 5.3 CPoured topagar onplate coverinsteadCopy andpastepsychopathUsing theP20 tipswith P200pipettePushing plungerto second stopon micro-pipettor whendrawing upliquidTurned overplateimmediateafter addingtop agarNOTE-TAKING!Tried to lightbunsenburner withgas turnedoffAccidentallythrowing awayimportanttubes orsamplesNofigurelegendsOnesentence ofbackgroundinformationDid not put filteron syringe forenrichedisolationmixtureTossinggloves andtubes intothe sharpsdisposalTurning dialto 005instead of050 for 5 uLusing a P10Labelingthe top ofthe plateLeft pipettepump rubberholder onpipetteNotspreadingthe top agarevenly onthe platePouring 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. Still brining drinks into the lab
  2. Handed in a lab report late
  3. Going up to 3 mL on serological pipette but using the wrong side to measure
  4. Dropped a pipette tip into tube full of liquid
  5. 100 101 102
  6. Could not light a bunsen burner
  7. Used diameter to calculate area instead of radius
  8. Sending lab reports for me to look at, at 12 AM
  9. Taking a picture of your spot test plate with tape still on
  10. Pushed too hard on syringe with filter
  11. Forgetting to take a picture of your plate
  12. Left top agar out too long and it solidified before pouring
  13. Forgetting lab coats
  14. Not recognizing you had phages on a spot test plate
  15. 100% plaque assay success rate
  16. Using bacteria and bacteriophage interchangeably
  17. Using a 10 mL serological pipette for 1 mL
  18. Using P200 instead of P20
  19. Not saying that H is for Hopey
  20. Using direct isolation for every method topic
  21. Getting contamination on spot plate and plaque assay
  22. Keep referencing Direct Isolation Protocol 5.3 C
  23. Poured top agar on plate cover instead
  24. Copy and paste psychopath
  25. Using the P20 tips with P200 pipette
  26. Pushing plunger to second stop on micro-pipettor when drawing up liquid
  27. Turned over plate immediate after adding top agar
  28. NOTE-TAKING!
  29. Tried to light bunsen burner with gas turned off
  30. Accidentally throwing away important tubes or samples
  31. No figure legends
  32. One sentence of background information
  33. Did not put filter on syringe for enriched isolation mixture
  34. Tossing gloves and tubes into the sharps disposal
  35. Turning dial to 005 instead of 050 for 5 uL using a P10
  36. Labeling the top of the plate
  37. Left pipette pump rubber holder on pipette
  38. Not spreading the top agar evenly on the plate
  39. Pouring the host bacteria onto a plate without adding top agar