Notrecognizingyou hadphages on aspot test plateTaking apicture ofyour spot testplate withtape still onLeft pipettepump rubberholder onpipetteUsing a 10mLserologicalpipette for 1mLStillbriningdrinks intothe labUsing directisolation foreverymethod topicUseddiameter tocalculatearea insteadof radiusAccidentallythrowing awayimportanttubes orsamplesCould notlight abunsenburnerTossinggloves andtubes intothe sharpsdisposalPushedtoo hardon syringewith filterForgettingto take apicture ofyour plateGettingcontaminationon spot plateand plaqueassayNOTE-TAKING!Turned overplateimmediateafter addingtop agarCopy andpastepsychopathGoing up to 3 mLon serologicalpipette but usingthe wrong side tomeasureTurning dialto 005instead of050 for 5 uLusing a P10Onesentence ofbackgroundinformationPushing plungerto second stopon micro-pipettor whendrawing upliquidUsingP200instead ofP20Poured topagar onplate coverinsteadDropped apipette tipinto tube fullof liquidPouring thehost bacteriaonto a platewithout addingtop agarTried to lightbunsenburner withgas turnedoffKeepreferencingDirectIsolationProtocol 5.3 C100% plaqueassaysuccess rateSending labreports forme to lookat, at 12 AMNofigurelegendsDid not put filteron syringe forenrichedisolationmixture100101102Forgettinglab coatsLeft top agarout too longand it solidifiedbefore pouringLabelingthe top ofthe plateUsing theP20 tipswith P200pipetteUsing bacteriaandbacteriophageinterchangeablyNotsayingthat H isfor HopeyHanded ina labreport lateNotspreadingthe top agarevenly onthe plateNotrecognizingyou hadphages on aspot test plateTaking apicture ofyour spot testplate withtape still onLeft pipettepump rubberholder onpipetteUsing a 10mLserologicalpipette for 1mLStillbriningdrinks intothe labUsing directisolation foreverymethod topicUseddiameter tocalculatearea insteadof radiusAccidentallythrowing awayimportanttubes orsamplesCould notlight abunsenburnerTossinggloves andtubes intothe sharpsdisposalPushedtoo hardon syringewith filterForgettingto take apicture ofyour plateGettingcontaminationon spot plateand plaqueassayNOTE-TAKING!Turned overplateimmediateafter addingtop agarCopy andpastepsychopathGoing up to 3 mLon serologicalpipette but usingthe wrong side tomeasureTurning dialto 005instead of050 for 5 uLusing a P10Onesentence ofbackgroundinformationPushing plungerto second stopon micro-pipettor whendrawing upliquidUsingP200instead ofP20Poured topagar onplate coverinsteadDropped apipette tipinto tube fullof liquidPouring thehost bacteriaonto a platewithout addingtop agarTried to lightbunsenburner withgas turnedoffKeepreferencingDirectIsolationProtocol 5.3 C100% plaqueassaysuccess rateSending labreports forme to lookat, at 12 AMNofigurelegendsDid not put filteron syringe forenrichedisolationmixture100101102Forgettinglab coatsLeft top agarout too longand it solidifiedbefore pouringLabelingthe top ofthe plateUsing theP20 tipswith P200pipetteUsing bacteriaandbacteriophageinterchangeablyNotsayingthat H isfor HopeyHanded ina labreport lateNotspreadingthe top agarevenly onthe plate

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