Pushing plungerto second stopon micro-pipettor whendrawing upliquidKeepreferencingDirectIsolationProtocol 5.3 CPouring thehost bacteriaonto a platewithout addingtop agarSending labreports forme to lookat, at 12 AMTossinggloves andtubes intothe sharpsdisposal100% plaqueassaysuccess rateLabelingthe top ofthe plateGoing up to 3 mLon serologicalpipette but usingthe wrong side tomeasureOnesentence ofbackgroundinformationUsing bacteriaandbacteriophageinterchangeablyUsing directisolation foreverymethod topicTried to lightbunsenburner withgas turnedoffPushedtoo hardon syringewith filterUsing a 10mLserologicalpipette for 1mLCould notlight abunsenburnerStillbriningdrinks intothe labNOTE-TAKING!Notspreadingthe top agarevenly onthe plateForgettinglab coatsLeft top agarout too longand it solidifiedbefore pouringUseddiameter tocalculatearea insteadof radiusHanded ina labreport latePoured topagar onplate coverinsteadGettingcontaminationon spot plateand plaqueassayUsing theP20 tipswith P200pipetteLeft pipettepump rubberholder onpipetteUsingP200instead ofP20Turning dialto 005instead of050 for 5 uLusing a P10Taking apicture ofyour spot testplate withtape still onTurned overplateimmediateafter addingtop agarAccidentallythrowing awayimportanttubes orsamplesNotrecognizingyou hadphages on aspot test plateNofigurelegendsNotsayingthat H isfor HopeyDropped apipette tipinto tube fullof liquidCopy andpastepsychopath100101102Forgettingto take apicture ofyour plateDid not put filteron syringe forenrichedisolationmixturePushing plungerto second stopon micro-pipettor whendrawing upliquidKeepreferencingDirectIsolationProtocol 5.3 CPouring thehost bacteriaonto a platewithout addingtop agarSending labreports forme to lookat, at 12 AMTossinggloves andtubes intothe sharpsdisposal100% plaqueassaysuccess rateLabelingthe top ofthe plateGoing up to 3 mLon serologicalpipette but usingthe wrong side tomeasureOnesentence ofbackgroundinformationUsing bacteriaandbacteriophageinterchangeablyUsing directisolation foreverymethod topicTried to lightbunsenburner withgas turnedoffPushedtoo hardon syringewith filterUsing a 10mLserologicalpipette for 1mLCould notlight abunsenburnerStillbriningdrinks intothe labNOTE-TAKING!Notspreadingthe top agarevenly onthe plateForgettinglab coatsLeft top agarout too longand it solidifiedbefore pouringUseddiameter tocalculatearea insteadof radiusHanded ina labreport latePoured topagar onplate coverinsteadGettingcontaminationon spot plateand plaqueassayUsing theP20 tipswith P200pipetteLeft pipettepump rubberholder onpipetteUsingP200instead ofP20Turning dialto 005instead of050 for 5 uLusing a P10Taking apicture ofyour spot testplate withtape still onTurned overplateimmediateafter addingtop agarAccidentallythrowing awayimportanttubes orsamplesNotrecognizingyou hadphages on aspot test plateNofigurelegendsNotsayingthat H isfor HopeyDropped apipette tipinto tube fullof liquidCopy andpastepsychopath100101102Forgettingto take apicture ofyour plateDid not put filteron syringe forenrichedisolationmixture

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