Pouring thehost bacteriaonto a platewithout addingtop agarPoured topagar onplate coverinsteadHanded ina labreport lateUsing a 10mLserologicalpipette for 1mLKeepreferencingDirectIsolationProtocol 5.3 CForgettinglab coatsNOTE-TAKING!Taking apicture ofyour spot testplate withtape still onTried to lightbunsenburner withgas turnedoffCopy andpastepsychopathStillbriningdrinks intothe labPushedtoo hardon syringewith filterGoing up to 3 mLon serologicalpipette but usingthe wrong side tomeasure100% plaqueassaysuccess ratePushing plungerto second stopon micro-pipettor whendrawing upliquidUsing bacteriaandbacteriophageinterchangeablyCould notlight abunsenburnerGettingcontaminationon spot plateand plaqueassayForgettingto take apicture ofyour plateDid not put filteron syringe forenrichedisolationmixtureLabelingthe top ofthe plateNofigurelegendsTurned overplateimmediateafter addingtop agarDropped apipette tipinto tube fullof liquidOnesentence ofbackgroundinformationNotsayingthat H isfor HopeyTossinggloves andtubes intothe sharpsdisposalLeft top agarout too longand it solidifiedbefore pouringNotspreadingthe top agarevenly onthe plateUseddiameter tocalculatearea insteadof radiusNotrecognizingyou hadphages on aspot test plateTurning dialto 005instead of050 for 5 uLusing a P10Left pipettepump rubberholder onpipetteUsing directisolation foreverymethod topicUsingP200instead ofP20Accidentallythrowing awayimportanttubes orsamplesUsing theP20 tipswith P200pipetteSending labreports forme to lookat, at 12 AM100101102Pouring thehost bacteriaonto a platewithout addingtop agarPoured topagar onplate coverinsteadHanded ina labreport lateUsing a 10mLserologicalpipette for 1mLKeepreferencingDirectIsolationProtocol 5.3 CForgettinglab coatsNOTE-TAKING!Taking apicture ofyour spot testplate withtape still onTried to lightbunsenburner withgas turnedoffCopy andpastepsychopathStillbriningdrinks intothe labPushedtoo hardon syringewith filterGoing up to 3 mLon serologicalpipette but usingthe wrong side tomeasure100% plaqueassaysuccess ratePushing plungerto second stopon micro-pipettor whendrawing upliquidUsing bacteriaandbacteriophageinterchangeablyCould notlight abunsenburnerGettingcontaminationon spot plateand plaqueassayForgettingto take apicture ofyour plateDid not put filteron syringe forenrichedisolationmixtureLabelingthe top ofthe plateNofigurelegendsTurned overplateimmediateafter addingtop agarDropped apipette tipinto tube fullof liquidOnesentence ofbackgroundinformationNotsayingthat H isfor HopeyTossinggloves andtubes intothe sharpsdisposalLeft top agarout too longand it solidifiedbefore pouringNotspreadingthe top agarevenly onthe plateUseddiameter tocalculatearea insteadof radiusNotrecognizingyou hadphages on aspot test plateTurning dialto 005instead of050 for 5 uLusing a P10Left pipettepump rubberholder onpipetteUsing directisolation foreverymethod topicUsingP200instead ofP20Accidentallythrowing awayimportanttubes orsamplesUsing theP20 tipswith P200pipetteSending labreports forme to lookat, at 12 AM100101102

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