Pushedtoo hardon syringewith filterDropped apipette tipinto tube fullof liquidUsing directisolation foreverymethod topicTaking apicture ofyour spot testplate withtape still onSending labreports forme to lookat, at 12 AM100101102Going up to 3 mLon serologicalpipette but usingthe wrong side tomeasureNOTE-TAKING!Did not put filteron syringe forenrichedisolationmixtureGettingcontaminationon spot plateand plaqueassayTurning dialto 005instead of050 for 5 uLusing a P10Accidentallythrowing awayimportanttubes orsamplesPouring thehost bacteriaonto a platewithout addingtop agarUsing bacteriaandbacteriophageinterchangeablyTried to lightbunsenburner withgas turnedoffKeepreferencingDirectIsolationProtocol 5.3 CLeft top agarout too longand it solidifiedbefore pouringForgettinglab coatsNofigurelegendsStillbriningdrinks intothe labPoured topagar onplate coverinsteadCould notlight abunsenburnerPushing plungerto second stopon micro-pipettor whendrawing upliquidForgettingto take apicture ofyour plateNotsayingthat H isfor HopeyOnesentence ofbackgroundinformationHanded ina labreport lateLeft pipettepump rubberholder onpipetteUsing a 10mLserologicalpipette for 1mLUseddiameter tocalculatearea insteadof radius100% plaqueassaysuccess rateUsing theP20 tipswith P200pipetteTurned overplateimmediateafter addingtop agarCopy andpastepsychopathNotspreadingthe top agarevenly onthe plateUsingP200instead ofP20Labelingthe top ofthe plateTossinggloves andtubes intothe sharpsdisposalNotrecognizingyou hadphages on aspot test platePushedtoo hardon syringewith filterDropped apipette tipinto tube fullof liquidUsing directisolation foreverymethod topicTaking apicture ofyour spot testplate withtape still onSending labreports forme to lookat, at 12 AM100101102Going up to 3 mLon serologicalpipette but usingthe wrong side tomeasureNOTE-TAKING!Did not put filteron syringe forenrichedisolationmixtureGettingcontaminationon spot plateand plaqueassayTurning dialto 005instead of050 for 5 uLusing a P10Accidentallythrowing awayimportanttubes orsamplesPouring thehost bacteriaonto a platewithout addingtop agarUsing bacteriaandbacteriophageinterchangeablyTried to lightbunsenburner withgas turnedoffKeepreferencingDirectIsolationProtocol 5.3 CLeft top agarout too longand it solidifiedbefore pouringForgettinglab coatsNofigurelegendsStillbriningdrinks intothe labPoured topagar onplate coverinsteadCould notlight abunsenburnerPushing plungerto second stopon micro-pipettor whendrawing upliquidForgettingto take apicture ofyour plateNotsayingthat H isfor HopeyOnesentence ofbackgroundinformationHanded ina labreport lateLeft pipettepump rubberholder onpipetteUsing a 10mLserologicalpipette for 1mLUseddiameter tocalculatearea insteadof radius100% plaqueassaysuccess rateUsing theP20 tipswith P200pipetteTurned overplateimmediateafter addingtop agarCopy andpastepsychopathNotspreadingthe top agarevenly onthe plateUsingP200instead ofP20Labelingthe top ofthe plateTossinggloves andtubes intothe sharpsdisposalNotrecognizingyou hadphages on aspot test plate

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