Going up to 3 mLon serologicalpipette but usingthe wrong side tomeasureCopy andpastepsychopathTurning dialto 005instead of050 for 5 uLusing a P10Could notlight abunsenburnerUsing bacteriaandbacteriophageinterchangeablyStillbriningdrinks intothe labUsing directisolation foreverymethod topicOnesentence ofbackgroundinformationDropped apipette tipinto tube fullof liquid100101102NofigurelegendsLeft top agarout too longand it solidifiedbefore pouringTurned overplateimmediateafter addingtop agarPoured topagar onplate coverinstead100% plaqueassaysuccess rateNotrecognizingyou hadphages on aspot test plateForgettingto take apicture ofyour plateTossinggloves andtubes intothe sharpsdisposalPushing plungerto second stopon micro-pipettor whendrawing upliquidAccidentallythrowing awayimportanttubes orsamplesPushedtoo hardon syringewith filterUsing a 10mLserologicalpipette for 1mLLabelingthe top ofthe plateUseddiameter tocalculatearea insteadof radiusUsingP200instead ofP20Left pipettepump rubberholder onpipetteNotspreadingthe top agarevenly onthe plateGettingcontaminationon spot plateand plaqueassayDid not put filteron syringe forenrichedisolationmixtureForgettinglab coatsSending labreports forme to lookat, at 12 AMNOTE-TAKING!Tried to lightbunsenburner withgas turnedoffHanded ina labreport lateNotsayingthat H isfor HopeyPouring thehost bacteriaonto a platewithout addingtop agarTaking apicture ofyour spot testplate withtape still onUsing theP20 tipswith P200pipetteKeepreferencingDirectIsolationProtocol 5.3 CGoing up to 3 mLon serologicalpipette but usingthe wrong side tomeasureCopy andpastepsychopathTurning dialto 005instead of050 for 5 uLusing a P10Could notlight abunsenburnerUsing bacteriaandbacteriophageinterchangeablyStillbriningdrinks intothe labUsing directisolation foreverymethod topicOnesentence ofbackgroundinformationDropped apipette tipinto tube fullof liquid100101102NofigurelegendsLeft top agarout too longand it solidifiedbefore pouringTurned overplateimmediateafter addingtop agarPoured topagar onplate coverinstead100% plaqueassaysuccess rateNotrecognizingyou hadphages on aspot test plateForgettingto take apicture ofyour plateTossinggloves andtubes intothe sharpsdisposalPushing plungerto second stopon micro-pipettor whendrawing upliquidAccidentallythrowing awayimportanttubes orsamplesPushedtoo hardon syringewith filterUsing a 10mLserologicalpipette for 1mLLabelingthe top ofthe plateUseddiameter tocalculatearea insteadof radiusUsingP200instead ofP20Left pipettepump rubberholder onpipetteNotspreadingthe top agarevenly onthe plateGettingcontaminationon spot plateand plaqueassayDid not put filteron syringe forenrichedisolationmixtureForgettinglab coatsSending labreports forme to lookat, at 12 AMNOTE-TAKING!Tried to lightbunsenburner withgas turnedoffHanded ina labreport lateNotsayingthat H isfor HopeyPouring thehost bacteriaonto a platewithout addingtop agarTaking apicture ofyour spot testplate withtape still onUsing theP20 tipswith P200pipetteKeepreferencingDirectIsolationProtocol 5.3 C

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