100101102Notsayingthat H isfor HopeyTurned overplateimmediateafter addingtop agarPoured topagar onplate coverinstead100% plaqueassaysuccess rateUsingP200instead ofP20Accidentallythrowing awayimportanttubes orsamplesDid not put filteron syringe forenrichedisolationmixtureNotspreadingthe top agarevenly onthe plateForgettinglab coatsUsing bacteriaandbacteriophageinterchangeablyDropped apipette tipinto tube fullof liquidLeft top agarout too longand it solidifiedbefore pouringUseddiameter tocalculatearea insteadof radiusSending labreports forme to lookat, at 12 AMTaking apicture ofyour spot testplate withtape still onTossinggloves andtubes intothe sharpsdisposalOnesentence ofbackgroundinformationNotrecognizingyou hadphages on aspot test plateNofigurelegendsPouring thehost bacteriaonto a platewithout addingtop agarUsing a 10mLserologicalpipette for 1mLKeepreferencingDirectIsolationProtocol 5.3 CStillbriningdrinks intothe labCould notlight abunsenburnerPushedtoo hardon syringewith filterCopy andpastepsychopathUsing theP20 tipswith P200pipetteUsing directisolation foreverymethod topicTurning dialto 005instead of050 for 5 uLusing a P10Labelingthe top ofthe plateHanded ina labreport lateLeft pipettepump rubberholder onpipetteNOTE-TAKING!Gettingcontaminationon spot plateand plaqueassayPushing plungerto second stopon micro-pipettor whendrawing upliquidForgettingto take apicture ofyour plateTried to lightbunsenburner withgas turnedoffGoing up to 3 mLon serologicalpipette but usingthe wrong side tomeasure100101102Notsayingthat H isfor HopeyTurned overplateimmediateafter addingtop agarPoured topagar onplate coverinstead100% plaqueassaysuccess rateUsingP200instead ofP20Accidentallythrowing awayimportanttubes orsamplesDid not put filteron syringe forenrichedisolationmixtureNotspreadingthe top agarevenly onthe plateForgettinglab coatsUsing bacteriaandbacteriophageinterchangeablyDropped apipette tipinto tube fullof liquidLeft top agarout too longand it solidifiedbefore pouringUseddiameter tocalculatearea insteadof radiusSending labreports forme to lookat, at 12 AMTaking apicture ofyour spot testplate withtape still onTossinggloves andtubes intothe sharpsdisposalOnesentence ofbackgroundinformationNotrecognizingyou hadphages on aspot test plateNofigurelegendsPouring thehost bacteriaonto a platewithout addingtop agarUsing a 10mLserologicalpipette for 1mLKeepreferencingDirectIsolationProtocol 5.3 CStillbriningdrinks intothe labCould notlight abunsenburnerPushedtoo hardon syringewith filterCopy andpastepsychopathUsing theP20 tipswith P200pipetteUsing directisolation foreverymethod topicTurning dialto 005instead of050 for 5 uLusing a P10Labelingthe top ofthe plateHanded ina labreport lateLeft pipettepump rubberholder onpipetteNOTE-TAKING!Gettingcontaminationon spot plateand plaqueassayPushing plungerto second stopon micro-pipettor whendrawing upliquidForgettingto take apicture ofyour plateTried to lightbunsenburner withgas turnedoffGoing up to 3 mLon serologicalpipette but usingthe wrong side tomeasure

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