Handed ina labreport lateUseddiameter tocalculatearea insteadof radiusTurning dialto 005instead of050 for 5 uLusing a P10Notsayingthat H isfor HopeyLeft pipettepump rubberholder onpipetteDid not put filteron syringe forenrichedisolationmixturePoured topagar onplate coverinsteadTossinggloves andtubes intothe sharpsdisposalNotrecognizingyou hadphages on aspot test plateForgettinglab coatsNOTE-TAKING!Left top agarout too longand it solidifiedbefore pouringUsing bacteriaandbacteriophageinterchangeablyStillbriningdrinks intothe labUsing directisolation foreverymethod topicDropped apipette tipinto tube fullof liquidTried to lightbunsenburner withgas turnedoffSending labreports forme to lookat, at 12 AM100% plaqueassaysuccess rateCopy andpastepsychopathTurned overplateimmediateafter addingtop agarGoing up to 3 mLon serologicalpipette but usingthe wrong side tomeasureAccidentallythrowing awayimportanttubes orsamplesLabelingthe top ofthe plateUsingP200instead ofP20100101102NofigurelegendsUsing a 10mLserologicalpipette for 1mLPouring thehost bacteriaonto a platewithout addingtop agarKeepreferencingDirectIsolationProtocol 5.3 CTaking apicture ofyour spot testplate withtape still onNotspreadingthe top agarevenly onthe platePushing plungerto second stopon micro-pipettor whendrawing upliquidPushedtoo hardon syringewith filterCould notlight abunsenburnerGettingcontaminationon spot plateand plaqueassayOnesentence ofbackgroundinformationUsing theP20 tipswith P200pipetteForgettingto take apicture ofyour plateHanded ina labreport lateUseddiameter tocalculatearea insteadof radiusTurning dialto 005instead of050 for 5 uLusing a P10Notsayingthat H isfor HopeyLeft pipettepump rubberholder onpipetteDid not put filteron syringe forenrichedisolationmixturePoured topagar onplate coverinsteadTossinggloves andtubes intothe sharpsdisposalNotrecognizingyou hadphages on aspot test plateForgettinglab coatsNOTE-TAKING!Left top agarout too longand it solidifiedbefore pouringUsing bacteriaandbacteriophageinterchangeablyStillbriningdrinks intothe labUsing directisolation foreverymethod topicDropped apipette tipinto tube fullof liquidTried to lightbunsenburner withgas turnedoffSending labreports forme to lookat, at 12 AM100% plaqueassaysuccess rateCopy andpastepsychopathTurned overplateimmediateafter addingtop agarGoing up to 3 mLon serologicalpipette but usingthe wrong side tomeasureAccidentallythrowing awayimportanttubes orsamplesLabelingthe top ofthe plateUsingP200instead ofP20100101102NofigurelegendsUsing a 10mLserologicalpipette for 1mLPouring thehost bacteriaonto a platewithout addingtop agarKeepreferencingDirectIsolationProtocol 5.3 CTaking apicture ofyour spot testplate withtape still onNotspreadingthe top agarevenly onthe platePushing plungerto second stopon micro-pipettor whendrawing upliquidPushedtoo hardon syringewith filterCould notlight abunsenburnerGettingcontaminationon spot plateand plaqueassayOnesentence ofbackgroundinformationUsing theP20 tipswith P200pipetteForgettingto take apicture ofyour 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. Handed in a lab report late
  2. Used diameter to calculate area instead of radius
  3. Turning dial to 005 instead of 050 for 5 uL using a P10
  4. Not saying that H is for Hopey
  5. Left pipette pump rubber holder on pipette
  6. Did not put filter on syringe for enriched isolation mixture
  7. Poured top agar on plate cover instead
  8. Tossing gloves and tubes into the sharps disposal
  9. Not recognizing you had phages on a spot test plate
  10. Forgetting lab coats
  11. NOTE-TAKING!
  12. Left top agar out too long and it solidified before pouring
  13. Using bacteria and bacteriophage interchangeably
  14. Still brining drinks into the lab
  15. Using direct isolation for every method topic
  16. Dropped a pipette tip into tube full of liquid
  17. Tried to light bunsen burner with gas turned off
  18. Sending lab reports for me to look at, at 12 AM
  19. 100% plaque assay success rate
  20. Copy and paste psychopath
  21. Turned over plate immediate after adding top agar
  22. Going up to 3 mL on serological pipette but using the wrong side to measure
  23. Accidentally throwing away important tubes or samples
  24. Labeling the top of the plate
  25. Using P200 instead of P20
  26. 100 101 102
  27. No figure legends
  28. Using a 10 mL serological pipette for 1 mL
  29. Pouring the host bacteria onto a plate without adding top agar
  30. Keep referencing Direct Isolation Protocol 5.3 C
  31. Taking a picture of your spot test plate with tape still on
  32. Not spreading the top agar evenly on the plate
  33. Pushing plunger to second stop on micro-pipettor when drawing up liquid
  34. Pushed too hard on syringe with filter
  35. Could not light a bunsen burner
  36. Getting contamination on spot plate and plaque assay
  37. One sentence of background information
  38. Using the P20 tips with P200 pipette
  39. Forgetting to take a picture of your plate