Media Mayhem
Sterile or Suspicious
Transformation Trouble
Purification Panic
Random Chaos
100

How many plates can be made from 500 mL of LB agar?

20 plates

100

What chemical and concentration is used to disinfect surfaces in the biosafety cabinet?

70% ethanol

100

What temperature is used for heat shock during transformation?

42°C

100

What detergent is present in the lysis buffer?

Triton X-100

100

What is the molecular weight of the HIV-p17?

16254.29 g/mol

200

If you are making a 100 ml stock solution of the premixed LB powder, how much LB powder should you use?

2.0 g (bottle says 20 g for 1 liter)

200

What should never be blocked inside the biosafety cabinet?

Air grille

200

How long do cells stay on ice before heat shock?

30 minutes

200

What temperature should centrifugation occur at during lysis?

4°C

200

How much sample is loaded into each well?

13-15 µL

300

What pH should minimal media be adjusted to?

pH 7.00–7.05

300

Your LB stock solution has turned a bit cloudy, what should you do?

assume it is contaminated, discard, and make a new stock of it

300

How long is the heat shock step?

30 seconds

300

What type of resin is used for purification?

Ni-NTA resin

300

What is the extinction coefficient for HIV-p17?

17085 M-1cm-1

400

What are the three ingredients needed to make LB media from scratch?

Tryptone, yeast extract, & Sodium chloride

400

Why are thiamine, biotin, and ampicillin sterile filtered instead of autoclaved?

They are heat sensitive

400

How much plasmid is added to competent cells?

1 µL

400

Which buffer has the second highest imidazole concentration?

Equilibration buffer (50 mM)

400

What voltage is used after the first 30 minutes in the electrophoresis step?

100V

500

What is the molecular weight of the ampicillin we use and what temperature do we store it at?

371.4 g/mol & -20 'C

500

What autoclave cycle should be used for liquid media?

Liquid 30 or 60

500

How much of the lysate do you save to be used for the gel?

100 uL

500

Why does imidazole help elute His-tagged protein?

it competes with histidine residues for nickel binding

500

Why are SDS and BME added to protein samples before running the gel?

SDS denatures proteins + gives uniform negative charge & BME breaks disulfide bonds