Turning dialto 005instead of050 for 5 uLusing a P10Notrecognizingyou hadphages on aspot test plateNofigurelegendsAccidentallythrowing awayimportanttubes orsamplesCould notlight abunsenburnerForgettingto take apicture ofyour plateNotsayingthat H isfor HopeyPouring thehost bacteriaonto a platewithout addingtop agarPushing plungerto second stopon micro-pipettor whendrawing upliquidUsing theP20 tipswith P200pipettePoured topagar onplate coverinsteadOnesentence ofbackgroundinformationLabelingthe top ofthe plateNotspreadingthe top agarevenly onthe plateUsing a 10mLserologicalpipette for 1mLPushedtoo hardon syringewith filterTried to lightbunsenburner withgas turnedoffSending labreports forme to lookat, at 12 AMDropped apipette tipinto tube fullof liquidKeepreferencingDirectIsolationProtocol 5.3 CCopy andpastepsychopath100% plaqueassaysuccess rateNOTE-TAKING!100101102Stillbriningdrinks intothe labHanded ina labreport lateLeft pipettepump rubberholder onpipetteGettingcontaminationon spot plateand plaqueassayTossinggloves andtubes intothe sharpsdisposalTaking apicture ofyour spot testplate withtape still onUsingP200instead ofP20Using directisolation foreverymethod topicUsing bacteriaandbacteriophageinterchangeablyForgettinglab coatsUseddiameter tocalculatearea insteadof radiusGoing up to 3 mLon serologicalpipette but usingthe wrong side tomeasureDid not put filteron syringe forenrichedisolationmixtureTurned overplateimmediateafter addingtop agarLeft top agarout too longand it solidifiedbefore pouringTurning dialto 005instead of050 for 5 uLusing a P10Notrecognizingyou hadphages on aspot test plateNofigurelegendsAccidentallythrowing awayimportanttubes orsamplesCould notlight abunsenburnerForgettingto take apicture ofyour plateNotsayingthat H isfor HopeyPouring thehost bacteriaonto a platewithout addingtop agarPushing plungerto second stopon micro-pipettor whendrawing upliquidUsing theP20 tipswith P200pipettePoured topagar onplate coverinsteadOnesentence ofbackgroundinformationLabelingthe top ofthe plateNotspreadingthe top agarevenly onthe plateUsing a 10mLserologicalpipette for 1mLPushedtoo hardon syringewith filterTried to lightbunsenburner withgas turnedoffSending labreports forme to lookat, at 12 AMDropped apipette tipinto tube fullof liquidKeepreferencingDirectIsolationProtocol 5.3 CCopy andpastepsychopath100% plaqueassaysuccess rateNOTE-TAKING!100101102Stillbriningdrinks intothe labHanded ina labreport lateLeft pipettepump rubberholder onpipetteGettingcontaminationon spot plateand plaqueassayTossinggloves andtubes intothe sharpsdisposalTaking apicture ofyour spot testplate withtape still onUsingP200instead ofP20Using directisolation foreverymethod topicUsing bacteriaandbacteriophageinterchangeablyForgettinglab coatsUseddiameter tocalculatearea insteadof radiusGoing up to 3 mLon serologicalpipette but usingthe wrong side tomeasureDid not put filteron syringe forenrichedisolationmixtureTurned overplateimmediateafter addingtop agarLeft top agarout too longand it solidifiedbefore pouring

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.


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