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This section describes the preparation of buffers and reagents used in the manipulation
of nucleic acids.
For preparation of acid and base stock solutions, see Tables A.2A.1 and A.2A.2 as well
as individual recipes.
GENERAL GUIDELINES
When preparing solutions, use deionized, distilled water and (for most applications)
reagents of the highest grade available. Sterilization is recommended for most applica-
tions and is generally accomplished by autoclaving. Materials with components that are
volatile, altered or damaged by heat, or whose pH or concentration are critical should be
sterilized by filtration through a 0.22-µm filter. In many cases such components are added
from concentrated stocks after the solution has been autoclaved. Where specialized
sterilization methods are required, this is indicated in the individual recipes.
CAUTION: It is important to follow laboratory safety guidelines and heed manufacturers’
precautions when working with hazardous chemicals; consult institutional safety officers
and appropriate references for further details.
STORAGE
Most simple stock solutions can be stored indefinitely at room temperature if reasonable
care is exercised to keep them sterile; where more rigorous conditions are required, this
is indicated in the individual recipes.
Table A.2A.1 Molarities and Specific Gravities of Concentrated Acids and Basesa
A.2A.2
Current Protocols in Food Analytical Chemistry
SELECTION OF BUFFERS
Table A.2A.2 reports pKa values for some common buffers. Note that polybasic buffers,
such as phosphoric acid and citric acid, have more than one useful pKa value. When
choosing a buffer, select a buffer material with a pKa close to the desired working pH (at
the desired concentration and temperature for use). In general, effective buffers have a
range of approximately 2 pH units centered about the pKa value. Ideally the dissociation
constant—and therefore the pH—should not shift with a change in concentration or
temperature. If the shift is small, as for MES and HEPES, then a concentrated stock
solution can be prepared and diluted without adjustment to the pH. Buffers containing
phosphate or citrate, however, show a significant shift in pH with concentration change,
and Tris buffers show a large change in pH with temperature. For convenience, concen-
trated stock solutions of these buffers can still be used, provided that a pH adjustment is
made after any temperature and concentration adjustments. All adjustments to pH should
be made using the appropriate base—usually NaOH or KOH, depending on the corre-
sponding free counterion. Tetramethylammonium hydroxide can be used to prepare
buffers without a mineral cation. Many common buffers are supplied both as a free acid
or base and as the corresponding salt. By mixing precalculated amounts of each, a series
of buffers with varying pH values can conveniently be prepared.
RECIPES
Ammonium acetate, 10 M
Dissolve 385.4 g ammonium acetate in 150 ml H2O
Add H2O to 500 ml
Sterilize by filtration
Citrate-phosphate buffer (McIlvaine’s buffer)
Solution A: 19.21 g/liter citric acid (0.1 M final)
Solution B: 53.65 g/liter Na2HPO4⋅7H2O or 71.7 g/liter Na2HPO4⋅12H2O
Referring to Table A.2A.3 for desired pH, mix the indicated volumes of solutions
A and B, then dilute with water to 100 ml. Filter sterilize, if necessary, using a 0.2
µm filter and store up to 1 month 4°C.
DTT (dithiothreitol), 1 M
Dissolve 1.55 g DTT in 10 ml water and filter sterilize. Store in aliquots at −20°C.
Do not autoclave to sterilize.
EDTA (ethylenediaminetetraacetic acid), 0.5 M (pH 8.0)
Dissolve 186.1 g disodium EDTA dihydrate in 700 ml water. Adjust pH to 8.0 with
10 M NaOH (∼50 ml; add slowly). Add water to 1 liter and filter sterilize.
Begin titrating before the sample is completely dissolved. EDTA, even in the disodium salt
form, is difficult to dissolve at this concentration unless the pH is increased to between 7
and 8. Heating the solution may also help to dissolve EDTA.
HCl, 1 M
Mix in the following order:
913.8 ml H2O
86.2 ml concentrated HCl (Table A.2A.1)
KCl, 1 M
74.6 g KCl
H2O to 1 liter Laboratory Stock
Solutions,
Equipment, and
Guidelines
A.2A.3
Current Protocols in Food Analytical Chemistry
MgCl2 , 1 M
20.3 g MgCl2⋅6H2O
H2O to 100 ml
MgCl2 is extremely hygroscopic. Do not store opened bottles for long periods of time.
MgSO4 , 1 M
24.6 g MgSO4⋅7H2O
H2O to 100 ml
NaCl, 5 M
292 g NaCl
H2O to 1 liter
NaOH, 10 M
Dissolve 400 g NaOH in 450 ml H2O
Add H2O to 1 liter
Potassium acetate buffer, 0.1 M
Solution A: 11.55 ml glacial acetic acid per liter (0.2 M) in water.
Solution B: 19.6 g potassium acetate (KC2H3O2) per liter (0.2 M) in water.
Referring to Table A.2A.4 for desired pH, mix the indicated volumes of solutions A
and B, then dilute with water to 100 ml. Filter sterilize if necessary. Store up to 3
months at room temperature.
This may be made as a 5- or 10-fold concentrate by scaling up the amount of sodium acetate
in the same volume. Acetate buffers show concentration-dependent pH changes, so check the
pH by diluting an aliquot of concentrate to the final concentration.
To prepare buffers with pH intermediate between the points listed in Table A.2A.4, prepare
closest higher pH, then titrate with solution A.
A.2A.4
Current Protocols in Food Analytical Chemistry
Table A.2A.4 Preparation of 0.1 M Sodium
and Potassium Acetate Buffersa
Laboratory Stock
Solutions,
Equipment, and
Guidelines
A.2A.5
Current Protocols in Food Analytical Chemistry
SDS, 20% (w/v)
Dissolve 20 g SDS (sodium dodecyl sulfate or sodium lauryl sulfate) in water to 100
ml total volume with stirring. Filter sterilize using a 0.45-µm filter.
It may be necessary to heat the solution slightly to fully dissolve the powder.
Sodium acetate, 3 M
Dissolve 408 g sodium acetate trihydrate (NaC2H3O2⋅3H2O) in 800 ml H2O
Adjust pH to 4.8, 5.0, or 5.2 (as desired) with 3 M acetic acid (see Table A.2A.1)
Add H2O to 1 liter
Filter sterilize
Sodium acetate buffer, 0.1 M
Solution A: 11.55 ml glacial acetic acid per liter (0.2 M) in water.
Solution B: 27.2 g sodium acetate (NaC2H3O2⋅3H2O) per liter (0.2 M) in water.
Referring to Table A.2A.4 for desired pH, mix the indicated volumes of solutions A
and B, then dilute with water to 100 ml. Filter sterilize if necessary. Store up to 3
months at room temperature.
This may be made as a 5- or 10-fold concentrate by scaling up the amount of sodium acetate
in the same volume. Acetate buffers show concentration-dependent pH changes, so check the
pH by diluting an aliquot of concentrate to the final concentration.
To prepare buffers with pH intermediate between the points listed in Table A.2A.4, prepare
closest higher pH, then titrate with solution A.
Sodium phosphate buffer, 0.1 M
Solution A: 27.6 g NaH2PO4⋅H2O per liter (0.2 M final) in water.
Solution B: 53.65 g Na2HPO4⋅7H2O per liter (0.2 M) in water.
Referring to Table A.2A.5 for desired pH, mix the indicated volumes of solutions A
and B, then dilute with water to 200 ml. Filter sterilize if necessary. Store up to 3
months at room temperature.
This buffer may be made as a 5- or 10-fold concentrate by scaling up the amount of sodium
phosphate in the same final volume. Phosphate buffers show concentration-dependent
changes in pH, so check the pH by diluting an aliquot of the concentrate to the final
concentration.
To prepare buffers with pH intermediate between the points listed in Table A.2A.5, prepare
closest higher pH, then titrate with solution A.
Tris⋅Cl, 1 M
Dissolve 121 g Tris base in 800 ml H2O
Adjust to desired pH with concentrated HCl
Adjust volume to 1 liter with H2O
Filter sterilize if necessary
Store up to 6 months at 4°C or room temperature
Approximately 70 ml HCl is needed to achieve a pH 7.4 solution, and ∼42 ml for a solution
that is pH 8.0.
IMPORTANT NOTE: The pH of Tris buffers changes significantly with temperature,
decreasing approximately 0.028 pH units per 1°C. Tris-buffered solutions should be adjusted
to the desired pH at the temperature at which they will be used. Because the pKa of Tris is
8.08, Tris should not be used as a buffer below pH ∼7.2 or above pH ∼9.0.
Always use high-quality Tris (lower-quality Tris can be recognized by its yellow appearance
when dissolved).
Common Buffers
and Stock
Solutions
A.2A.6
Current Protocols in Food Analytical Chemistry
LITERATURE CITED
Chemical Rubber Company, 1975. CRC Handbook of Biochemistry and Molecular Biology, Physical and
Chemical Data, 3d ed., Vol. 1. CRC Press, Boca Raton, Fla.
Fasman, G.D. (ed.) 1989. Practical Handbook of Biochemistry and Molecular Biology. CRC Press, Boca
Raton, Fla.
Mohan, C. (ed.), 1997. Buffers: A Guide for the Preparation and Use of Buffers in Biological Systems,
Calbiochem, San Diego, Calif.
Laboratory Stock
Solutions,
Equipment, and
Guidelines
A.2A.7
Current Protocols in Food Analytical Chemistry