Onesentence ofbackgroundinformationGettingcontaminationon spot plateand plaqueassayUsing directisolation foreverymethod topic100101102Labelingthe top ofthe plateTried to lightbunsenburner withgas turnedoffPouring thehost bacteriaonto a platewithout addingtop agarSending labreports forme to lookat, at 12 AMStillbriningdrinks intothe labLeft pipettepump rubberholder onpipetteLeft top agarout too longand it solidifiedbefore pouringGoing up to 3 mLon serologicalpipette but usingthe wrong side tomeasureKeepreferencingDirectIsolationProtocol 5.3 CTurned overplateimmediateafter addingtop agarPoured topagar onplate coverinsteadNofigurelegendsUseddiameter tocalculatearea insteadof radiusUsing bacteriaandbacteriophageinterchangeablyNOTE-TAKING!Notsayingthat H isfor HopeyForgettinglab coatsNotrecognizingyou hadphages on aspot test plateUsing a 10mLserologicalpipette for 1mLNotspreadingthe top agarevenly onthe platePushedtoo hardon syringewith filterDid not put filteron syringe forenrichedisolationmixtureAccidentallythrowing awayimportanttubes orsamplesForgettingto take apicture ofyour plateTossinggloves andtubes intothe sharpsdisposalPushing plungerto second stopon micro-pipettor whendrawing upliquidDropped apipette tipinto tube fullof liquidTurning dialto 005instead of050 for 5 uLusing a P10Could notlight abunsenburnerCopy andpastepsychopathHanded ina labreport late100% plaqueassaysuccess rateUsing theP20 tipswith P200pipetteTaking apicture ofyour spot testplate withtape still onUsingP200instead ofP20Onesentence ofbackgroundinformationGettingcontaminationon spot plateand plaqueassayUsing directisolation foreverymethod topic100101102Labelingthe top ofthe plateTried to lightbunsenburner withgas turnedoffPouring thehost bacteriaonto a platewithout addingtop agarSending labreports forme to lookat, at 12 AMStillbriningdrinks intothe labLeft pipettepump rubberholder onpipetteLeft top agarout too longand it solidifiedbefore pouringGoing up to 3 mLon serologicalpipette but usingthe wrong side tomeasureKeepreferencingDirectIsolationProtocol 5.3 CTurned overplateimmediateafter addingtop agarPoured topagar onplate coverinsteadNofigurelegendsUseddiameter tocalculatearea insteadof radiusUsing bacteriaandbacteriophageinterchangeablyNOTE-TAKING!Notsayingthat H isfor HopeyForgettinglab coatsNotrecognizingyou hadphages on aspot test plateUsing a 10mLserologicalpipette for 1mLNotspreadingthe top agarevenly onthe platePushedtoo hardon syringewith filterDid not put filteron syringe forenrichedisolationmixtureAccidentallythrowing awayimportanttubes orsamplesForgettingto take apicture ofyour plateTossinggloves andtubes intothe sharpsdisposalPushing plungerto second stopon micro-pipettor whendrawing upliquidDropped apipette tipinto tube fullof liquidTurning dialto 005instead of050 for 5 uLusing a P10Could notlight abunsenburnerCopy andpastepsychopathHanded ina labreport late100% plaqueassaysuccess rateUsing theP20 tipswith P200pipetteTaking apicture ofyour spot testplate withtape still onUsingP200instead ofP20

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