Pushing plungerto second stopon micro-pipettor whendrawing upliquidCopy andpastepsychopathHanded ina labreport late100% plaqueassaysuccess ratePouring thehost bacteriaonto a platewithout addingtop agarAccidentallythrowing awayimportanttubes orsamplesNotrecognizingyou hadphages on aspot test plateUsing directisolation foreverymethod topicTossinggloves andtubes intothe sharpsdisposalLeft pipettepump rubberholder onpipetteNofigurelegendsTurning dialto 005instead of050 for 5 uLusing a P10Going up to 3 mLon serologicalpipette but usingthe wrong side tomeasureStillbriningdrinks intothe labForgettinglab coatsUsing bacteriaandbacteriophageinterchangeablyLabelingthe top ofthe plateTried to lightbunsenburner withgas turnedoffOnesentence ofbackgroundinformationUseddiameter tocalculatearea insteadof radius100101102Gettingcontaminationon spot plateand plaqueassayTurned overplateimmediateafter addingtop agarKeepreferencingDirectIsolationProtocol 5.3 CUsing a 10mLserologicalpipette for 1mLDropped apipette tipinto tube fullof liquidUsing theP20 tipswith P200pipetteSending labreports forme to lookat, at 12 AMLeft top agarout too longand it solidifiedbefore pouringPushedtoo hardon syringewith filterNOTE-TAKING!Poured topagar onplate coverinsteadTaking apicture ofyour spot testplate withtape still onNotspreadingthe top agarevenly onthe plateDid not put filteron syringe forenrichedisolationmixtureNotsayingthat H isfor HopeyForgettingto take apicture ofyour plateUsingP200instead ofP20Could notlight abunsenburnerPushing plungerto second stopon micro-pipettor whendrawing upliquidCopy andpastepsychopathHanded ina labreport late100% plaqueassaysuccess ratePouring thehost bacteriaonto a platewithout addingtop agarAccidentallythrowing awayimportanttubes orsamplesNotrecognizingyou hadphages on aspot test plateUsing directisolation foreverymethod topicTossinggloves andtubes intothe sharpsdisposalLeft pipettepump rubberholder onpipetteNofigurelegendsTurning dialto 005instead of050 for 5 uLusing a P10Going up to 3 mLon serologicalpipette but usingthe wrong side tomeasureStillbriningdrinks intothe labForgettinglab coatsUsing bacteriaandbacteriophageinterchangeablyLabelingthe top ofthe plateTried to lightbunsenburner withgas turnedoffOnesentence ofbackgroundinformationUseddiameter tocalculatearea insteadof radius100101102Gettingcontaminationon spot plateand plaqueassayTurned overplateimmediateafter addingtop agarKeepreferencingDirectIsolationProtocol 5.3 CUsing a 10mLserologicalpipette for 1mLDropped apipette tipinto tube fullof liquidUsing theP20 tipswith P200pipetteSending labreports forme to lookat, at 12 AMLeft top agarout too longand it solidifiedbefore pouringPushedtoo hardon syringewith filterNOTE-TAKING!Poured topagar onplate coverinsteadTaking apicture ofyour spot testplate withtape still onNotspreadingthe top agarevenly onthe plateDid not put filteron syringe forenrichedisolationmixtureNotsayingthat H isfor HopeyForgettingto take apicture ofyour plateUsingP200instead ofP20Could notlight abunsenburner

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