Sending labreports forme to lookat, at 12 AMGoing up to 3 mLon serologicalpipette but usingthe wrong side tomeasureUsingP200instead ofP20Accidentallythrowing awayimportanttubes orsamplesNofigurelegendsOnesentence ofbackgroundinformationTaking apicture ofyour spot testplate withtape still onForgettinglab coatsNotsayingthat H isfor HopeyPushedtoo hardon syringewith filterTried to lightbunsenburner withgas turnedoffUseddiameter tocalculatearea insteadof radiusTurning dialto 005instead of050 for 5 uLusing a P10Stillbriningdrinks intothe labNOTE-TAKING!Using theP20 tipswith P200pipettePushing plungerto second stopon micro-pipettor whendrawing upliquidNotrecognizingyou hadphages on aspot test plateDropped apipette tipinto tube fullof liquidNotspreadingthe top agarevenly onthe plateUsing bacteriaandbacteriophageinterchangeablyForgettingto take apicture ofyour plateKeepreferencingDirectIsolationProtocol 5.3 CGettingcontaminationon spot plateand plaqueassayUsing directisolation foreverymethod topicLeft top agarout too longand it solidifiedbefore pouringTurned overplateimmediateafter addingtop agarHanded ina labreport lateDid not put filteron syringe forenrichedisolationmixturePouring thehost bacteriaonto a platewithout addingtop agarLeft pipettepump rubberholder onpipetteCopy andpastepsychopath100% plaqueassaysuccess rateCould notlight abunsenburnerTossinggloves andtubes intothe sharpsdisposalUsing a 10mLserologicalpipette for 1mLLabelingthe top ofthe plate100101102Poured topagar onplate coverinsteadSending labreports forme to lookat, at 12 AMGoing up to 3 mLon serologicalpipette but usingthe wrong side tomeasureUsingP200instead ofP20Accidentallythrowing awayimportanttubes orsamplesNofigurelegendsOnesentence ofbackgroundinformationTaking apicture ofyour spot testplate withtape still onForgettinglab coatsNotsayingthat H isfor HopeyPushedtoo hardon syringewith filterTried to lightbunsenburner withgas turnedoffUseddiameter tocalculatearea insteadof radiusTurning dialto 005instead of050 for 5 uLusing a P10Stillbriningdrinks intothe labNOTE-TAKING!Using theP20 tipswith P200pipettePushing plungerto second stopon micro-pipettor whendrawing upliquidNotrecognizingyou hadphages on aspot test plateDropped apipette tipinto tube fullof liquidNotspreadingthe top agarevenly onthe plateUsing bacteriaandbacteriophageinterchangeablyForgettingto take apicture ofyour plateKeepreferencingDirectIsolationProtocol 5.3 CGettingcontaminationon spot plateand plaqueassayUsing directisolation foreverymethod topicLeft top agarout too longand it solidifiedbefore pouringTurned overplateimmediateafter addingtop agarHanded ina labreport lateDid not put filteron syringe forenrichedisolationmixturePouring thehost bacteriaonto a platewithout addingtop agarLeft pipettepump rubberholder onpipetteCopy andpastepsychopath100% plaqueassaysuccess rateCould notlight abunsenburnerTossinggloves andtubes intothe sharpsdisposalUsing a 10mLserologicalpipette for 1mLLabelingthe top ofthe plate100101102Poured topagar onplate coverinstead

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