Gettingcontaminationon spot plateand plaqueassayOnesentence ofbackgroundinformationTaking apicture ofyour spot testplate withtape still onPoured topagar onplate coverinsteadCould notlight abunsenburnerLeft pipettepump rubberholder onpipetteTurning dialto 005instead of050 for 5 uLusing a P10Turned overplateimmediateafter addingtop agarGoing up to 3 mLon serologicalpipette but usingthe wrong side tomeasurePouring thehost bacteriaonto a platewithout addingtop agarForgettingto take apicture ofyour platePushing plungerto second stopon micro-pipettor whendrawing upliquidUsingP200instead ofP20Pushedtoo hardon syringewith filterCopy andpastepsychopath100101102Stillbriningdrinks intothe labNOTE-TAKING!Using a 10mLserologicalpipette for 1mLDropped apipette tipinto tube fullof liquidAccidentallythrowing awayimportanttubes orsamplesLeft top agarout too longand it solidifiedbefore pouringUsing theP20 tipswith P200pipetteNotspreadingthe top agarevenly onthe plateUsing bacteriaandbacteriophageinterchangeablyUsing directisolation foreverymethod topicTried to lightbunsenburner withgas turnedoffNofigurelegendsForgettinglab coatsUseddiameter tocalculatearea insteadof radiusDid not put filteron syringe forenrichedisolationmixture100% plaqueassaysuccess rateLabelingthe top ofthe plateSending labreports forme to lookat, at 12 AMTossinggloves andtubes intothe sharpsdisposalKeepreferencingDirectIsolationProtocol 5.3 CNotrecognizingyou hadphages on aspot test plateNotsayingthat H isfor HopeyHanded ina labreport lateGettingcontaminationon spot plateand plaqueassayOnesentence ofbackgroundinformationTaking apicture ofyour spot testplate withtape still onPoured topagar onplate coverinsteadCould notlight abunsenburnerLeft pipettepump rubberholder onpipetteTurning dialto 005instead of050 for 5 uLusing a P10Turned overplateimmediateafter addingtop agarGoing up to 3 mLon serologicalpipette but usingthe wrong side tomeasurePouring thehost bacteriaonto a platewithout addingtop agarForgettingto take apicture ofyour platePushing plungerto second stopon micro-pipettor whendrawing upliquidUsingP200instead ofP20Pushedtoo hardon syringewith filterCopy andpastepsychopath100101102Stillbriningdrinks intothe labNOTE-TAKING!Using a 10mLserologicalpipette for 1mLDropped apipette tipinto tube fullof liquidAccidentallythrowing awayimportanttubes orsamplesLeft top agarout too longand it solidifiedbefore pouringUsing theP20 tipswith P200pipetteNotspreadingthe top agarevenly onthe plateUsing bacteriaandbacteriophageinterchangeablyUsing directisolation foreverymethod topicTried to lightbunsenburner withgas turnedoffNofigurelegendsForgettinglab coatsUseddiameter tocalculatearea insteadof radiusDid not put filteron syringe forenrichedisolationmixture100% plaqueassaysuccess rateLabelingthe top ofthe plateSending labreports forme to lookat, at 12 AMTossinggloves andtubes intothe sharpsdisposalKeepreferencingDirectIsolationProtocol 5.3 CNotrecognizingyou hadphages on aspot test plateNotsayingthat H isfor HopeyHanded ina labreport late

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