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