Ran gel backwards Forgot to turn the gel on Too short elongation time Band in the negative control Primer insertion Too high voltage, gel liquified No band in the positive control Wrong annealing temp Forgot gel stain Wrong PCR program Didn't mix with sample buffer Used protein marker as DNA ladder Sample spillover into next lane Frameshift mutation Wrong salt/buffer concentration Not enough mastermix Multiple annealing sites Prepared agarose gel with dH2O Forgot marker Ran gel too long Forgot template Didn't mix properly Wrong primers Spilled the sample Ran gel backwards Forgot to turn the gel on Too short elongation time Band in the negative control Primer insertion Too high voltage, gel liquified No band in the positive control Wrong annealing temp Forgot gel stain Wrong PCR program Didn't mix with sample buffer Used protein marker as DNA ladder Sample spillover into next lane Frameshift mutation Wrong salt/buffer concentration Not enough mastermix Multiple annealing sites Prepared agarose gel with dH2O Forgot marker Ran gel too long Forgot template Didn't mix properly Wrong primers Spilled the sample
(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.
Ran gel backwards
Forgot to turn the gel on
Too short elongation time
Band in the negative control
Primer insertion
Too high voltage, gel liquified
No band in the positive control
Wrong annealing temp
Forgot gel stain
Wrong
PCR program
Didn't mix with sample buffer
Used protein marker as DNA ladder
Sample spillover into next lane
Frameshift mutation
Wrong
salt/buffer concentration
Not enough mastermix
Multiple annealing sites
Prepared agarose gel with dH2O
Forgot marker
Ran gel too long
Forgot template
Didn't mix properly
Wrong primers
Spilled the sample