Common Lab Solutions
- General notes
about making solutions:
- 1. In general gloves, coat, and eye protection should be worn
when making up solutions. To avoid noxious fumes or spills,
dispense concentrated acids and bases in the fume hood. Only
small volume container of acid and base solutions should be used at the
pH meter.
- 1. Use clean baked (foil covered) beakers for mixing solutions
(0.1 - 1L). Smaller volumes solutions can be mixed in 15 or 50 mL
sterile disposable conical tubes. Large volume solutions (7 -8 L)
are less precise and can be made directly in their carboy containers.
- 2. Use high quality filtered water for all laboratory
solutions.
- 3. Measure powders into a disposable weigh boat. Use clean
sterile spoons or scoopulas sparingly. Discard excess material do
not return it to the stock containers.
- 4. If solutions need to be pH'd then only add 80% of the volume
of H2O needed prior to pHing to be sure that the final volume is not
exceeded.
- 5. After all of the chemicals have been added transfer the
solution to a 0.5 or 1.0 L graduated cylinder and q.s. with H2O.
- 6. Divide (0.5 or 1L) solutions into sterile 500 mL media bottles
prior to autoclaving (if directed). Small volume
solutions are sterilized by filtration with a sterile syringe and
syringe tip 0.25 µm filters. Larger volume solutions should
be filtered on bottle top filters in a tissue culture hood if their
ingredients are heat sensitive (e.g. tissue culture media).
- Ampicillin (50 mg/mL stock)
- 5 g. Ampicillin
- 100 mL H2O
- Filter sterilize in 1.5 mL aliquots
- Store at -20°C
-
- Bacteria plates (Makes 30 plates per 1 L)
- 1 L. LB media (See below)
- 15 g. Bacto-agar (for plates, use 7.5 gm for top agar)
- Autoclave in a large (e.g. 2L flask)
- Cool flask to 55°C in a water bath
- Add antibiotics when media is < 55°C (not too hot to
handle)
- Lay empty dishes on a benchtop.
- Use a glove and quickly pour enough LB agar into each dish to
cover the plate (or ~4 mm thick.)
- Avoid tipping the flask repeatedly to mimimize foaming
- Pass a Bunsen burner flame over open plates to pop air bubbles
- Partially cover plates with their lids untill they cool off and
harden
- Leave plates at room temperature overnight to allow condensation
to evaporate from lids
- Stack plates and mark them to indicate the type of
antibiotic. Store them at 4ºC in the original plastic sleeve
- Coomassie Blue Stain (1 L)
- 2.5 g. Coomassie brilliant blue
- 500 mL Methanol
- 425 mL H2O
- 75 mL glacial acetic acid
-
- Destain (5 L)
- 500 mL Methanol
- 500 mL Glacial Acetic acid
- 4 L H2O
-
- EDTA (0.5 M)
- 186.1 g. EDTA (disodium salt)
- 700 mL H2O
- pH to 8.0 with 10N NaOH (this helps to dissolve the EDTA)
- q.s. 1 L. H2O
- Sterilize by autoclaving
-
- LB Medium (per 1 L)
- 10 g. Bacto-tryptone
- 5 g. Bacto-yeast extract
- 10 g. NaCl
- Adjust pH to 7.5 with NaOH
- q.s. H2O
- Sterilize by autoclaving
-
- 5M NaCl
- 146 g NaCl
- q.s. to 500 mL with H2O
- Sterilize by autoclaving
-
- 10x PBS, pH=7.4 (per 1 L)
- 1.44 g. KH2PO4 (Potassium Phosphate
monobasic) (MW = 136 g/mole)
- 90 g. NaCl (MW = 58 g/mole)
- 7.95 g. Na2HPO4-7H2O (Sodium
Phosphate dibasic) (MW = 268 g/mole)
- q.s. to 1 L with H2O.
- Sterilize by autoclaving.
- SDS running buffer, 10x - make directly in 8 L
carboy.
- 1.0 kg Glycine
- 140 g. Tris base
- 70 g. SDS
-
- 10% SDS
- 50 g. Sodium Lauryl sulfate (Sigma L-5750)
- q.s. to 0.5 L. with H2O
-
- SSC, 20x (3M NaCl, 0.3M Citrate)
- 175 g NaCl
- 88.2 g NaCitrate
- pH to 7.4 with NaOH or HCl
- q.s. to 1 L. with H2O
-
- TBE, 5x (8 L) - make directly in 8 L carboy.
- 432 g Tris base
- 220 g Boric acid
- 37.2 g EDTA (disodium salt)
- (or 160 mL 0.5 M EDTA)
- q.s. 8 L. H2O
-
- 0.5% TNT (8 L) - make directly in 8 L carboy.
- 240 mL 5 M NaCl
- 100 mL 2M Tris pH7.5
- 400 mL 10 % v/v Tween 20 [0.5% v/v final]
- 7.26 L H2O
-
- Tris pH 7.4 (or pH 8.0)
- 60.5 g. Tris Base
- 400 mL H2O
- pH to 7.4 (or 8.0) with conc. HCl
- q.s. to 500 mL with H2O
-
- Western Transfer Solution (A) - make directly in 8 L
carboy.
- 24 g. Tris-base [25 mM final]
- 1.66 L Isopropanol [20% v/v final]
- 42.4 g. e-aminocaproic acid [40 mM final]
- q.s. 8 L. H2O
-
- Western Transfer Solution (B) - make directly in 8
L carboy.
- 24 g. Tris-base [25 mM final]
- 1.66 L Isopropanol [20% v/v final]
- q.s. 8 L. H2O
-
- Western Transfer Solution (C) - make directly in 8
L carboy.
- 242.4 g. Tris-base [250 mM final]
- 1.66 L. Isopropanol [20% v/v final]
- q.s. 8 L. H2O
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