Labelingthe top ofthe plateHanded ina labreport latePouring thehost bacteriaonto a platewithout addingtop agarUsing a 10mLserologicalpipette for 1mLStillbriningdrinks intothe labGoing up to 3 mLon serologicalpipette but usingthe wrong side tomeasureNOTE-TAKING!Left top agarout too longand it solidifiedbefore pouringPushedtoo hardon syringewith filterTurning dialto 005instead of050 for 5 uLusing a P10Pushing plungerto second stopon micro-pipettor whendrawing upliquid100101102Turned overplateimmediateafter addingtop agarUsing directisolation foreverymethod topicTried to lightbunsenburner withgas turnedoffLeft pipettepump rubberholder onpipetteForgettingto take apicture ofyour plateUsingP200instead ofP20Taking apicture ofyour spot testplate withtape still onAccidentallythrowing awayimportanttubes orsamplesTossinggloves andtubes intothe sharpsdisposalCould notlight abunsenburnerNotrecognizingyou hadphages on aspot test plateGettingcontaminationon spot plateand plaqueassayUsing theP20 tipswith P200pipetteNofigurelegendsOnesentence ofbackgroundinformationNotsayingthat H isfor HopeyUseddiameter tocalculatearea insteadof radiusNotspreadingthe top agarevenly onthe plateUsing bacteriaandbacteriophageinterchangeablyPoured topagar onplate coverinstead100% plaqueassaysuccess rateKeepreferencingDirectIsolationProtocol 5.3 CDropped apipette tipinto tube fullof liquidSending labreports forme to lookat, at 12 AMDid not put filteron syringe forenrichedisolationmixtureCopy andpastepsychopathForgettinglab coatsLabelingthe top ofthe plateHanded ina labreport latePouring thehost bacteriaonto a platewithout addingtop agarUsing a 10mLserologicalpipette for 1mLStillbriningdrinks intothe labGoing up to 3 mLon serologicalpipette but usingthe wrong side tomeasureNOTE-TAKING!Left top agarout too longand it solidifiedbefore pouringPushedtoo hardon syringewith filterTurning dialto 005instead of050 for 5 uLusing a P10Pushing plungerto second stopon micro-pipettor whendrawing upliquid100101102Turned overplateimmediateafter addingtop agarUsing directisolation foreverymethod topicTried to lightbunsenburner withgas turnedoffLeft pipettepump rubberholder onpipetteForgettingto take apicture ofyour plateUsingP200instead ofP20Taking apicture ofyour spot testplate withtape still onAccidentallythrowing awayimportanttubes orsamplesTossinggloves andtubes intothe sharpsdisposalCould notlight abunsenburnerNotrecognizingyou hadphages on aspot test plateGettingcontaminationon spot plateand plaqueassayUsing theP20 tipswith P200pipetteNofigurelegendsOnesentence ofbackgroundinformationNotsayingthat H isfor HopeyUseddiameter tocalculatearea insteadof radiusNotspreadingthe top agarevenly onthe plateUsing bacteriaandbacteriophageinterchangeablyPoured topagar onplate coverinstead100% plaqueassaysuccess rateKeepreferencingDirectIsolationProtocol 5.3 CDropped apipette tipinto tube fullof liquidSending labreports forme to lookat, at 12 AMDid not put filteron syringe forenrichedisolationmixtureCopy andpastepsychopathForgettinglab coats

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