ZÁKLADNI ROZTOKY POUŽÍVANE V MOLEKULÁRNI BIOLOGII TAB££ B.7 (continued) Solution Method, of preparation Comments 0.1 m Adenosine triphosphate (ATP) 10 M Ammonium acetate 10% Ammonium persulfate BCIP 2 x BES-buffered saline 1 h CaCla 2.5 M CaCl, Deoxyribonucleoside triphosphates (dNTPs) Dissolve 60 mg of ATP in 0.8 ml of H20. Adjust the pH to 7.0 with 0.1 n NaOH. Adjust the volume to 1 ml with distilled HsO. Dispense the solution into small aliquots and store at -70°C. Dissolve 770 g of ammonium acetate in 800 ml of H20. Adjust the volume to 1 liter with HaO. Sterilize by filtration. To 1 g of ammonium persulfate, add H20 to 10 ml. The solution may be stored for several weeks at 4°C. Dissolve 0.5 g of 5-bromo-4~chloro-3-indolyl phosphate disodium salt, which is available from several manufacturers, in 10 ml of 100% dimethylformamide. Store at i"C Dissolve 1.07 g of BES uV,N-bis[2-hydroxy-ethyl]-2-aminoethanesulfonic acid), 1.6 g of NaCl, and 0.027 g of Na2HP04 in a total volume of 90 ml of distilled H20. Adjust the pH of the solution to 6.96 with HCl at room temperature, and then adjust the volume to 100 ml with distilled H20. Sterilize the solution by passage through a 0.22-micron filter, and store in aliquots at — 20°C. Dissolve 54 g of CaCl;, - 6H20 in 200 ml of pure HsO (Milli-Q or equivalent). Sterilize the solution by passage through a 0.22-micron filter. Store in 1-ml aliquots at — 206C. Dissolve 13-5 g of CaCl2 ■ 6H20 in 20 ml of distilled H20. Sterilize the solution by passage through a 0.22-micron filter. Store in 1-ml aliquots at -20°C. Dissolve each dNTP in H20 at an approximate concentration of 100 mM. Using 0.05 m Tris base and a micropipette, adjust the pH of each of the solutions to 7.0 (use pH paper to check the pH). Dilute an aliquot of the neutralized dNTP appropriately, and read the optical density at the wavelengths given in the table Initially, the BCIP may not dissolve completely (especially if the dimethylformamide is not very fresh). If this occurs, vortex the mixture to suspend the BCIP and then withdraw the desired amount using a pipette tip cut off to make a large bore. The BCIP will dissolve fully in the next step of the protocol. When preparing competent cells, thaw an aliquot and dilute it to 100 ml with pure H20. Sterilize the solution by filtration through a Nalgene filter (0.45-micron pore size), and then chill it to 0°C. 1 M Dithiothreitol (DVT) 0.5 m EDTA (pH 8.0) Ethidium bromide (10 mg/ml) 2x HEPES-buffered saline IPTG below. Calculate the actual concentration of each dNTP. Dilute the solutions with H20 to a final concentration of 50 idm dNTP, Store each separately at — 70°C in small aliquots. Extinction Wavelength Coefficient (fi Base (nm) (m_1 cm"1) A 259 1.54x10* G 253 1.37 xlO4 C 271 9.10 xlO3 T 260 7.40 x 10a For a cuvette with a path length of 1 cm, absorbance = cm. 100 iriM stock solutions of each dNTP are commercially available (Pharmacia) if you do not want to prepare your own. Dissolve 3.09 g of DTT in 20 ml of 0.01 m sodium acetate (pH 5.2). Sterilize by filtration. Dispense into 1-ml aliquots and store _i -20°C. Add 186.1 g of disodium ethylenediaminetetra-acetate - 2HE0 to 800 ml of H20. Stir vigorously on a magnetic stirrer. Adjust the pH to 8.0 with NaOH (-20 g of NaOH pellets). Dispense into aliquots and sterilize by auto-claving. Add 1 g of ethidium bromide to 100 ml of H20. Stir on a magnetic stirrer for several hours to ensure that the dye has dissolved. Wrap the container in aluminum foil or transfer the solution to a dark bottle and store at room temperature. Dissolve 1.6 g of NaCl, 0.074 g of KCl, 0.027 g of Na2HPO„ ■ 2H20, 0.2 g of dextrose, and 1 g of HEPES in a total volume of 90 ml of distilled HsO. Adjust the pH to 7.05 with 0.5 n NaOH, and then adjust the volume to 100 ml with distilled H20. Sterilize the solution by passage through a 0.22-micron filter. Store in 5-ml aliquots at -20°C. Isopropylthio-ß-D-galactoside (m.w, = 238.3). Make a solution of IPTG by dissolving 2 g of IPTG in 8 ml of distilled H20. Adjust the volume of the solution to 10 ml with distilled HjO and sterilize by filtration through a 0.22-micron disposable filter. Dispense the solution into 1-ml aliquots and store them at -20°C. Do not autoclave DTT or solutions containing DDT. The disodium salt of EDTA will not go into solution until the pH of the solution is adjusted to approximately 8.0 by the addition of NaOH. Caution: Ethidium bromide is a powerful mutagen and is moderately toxic. Gloves should be worn when working with solutions that contain this dye, and a mask should be worn when weighing it out. After use, these solutions should be decontaminated by one of the methods described in Appendix E. S.7 (continued) Solution Method of preparation Comments 1 m Magnesium acetate 1 m MgCI2 ß- Mercaptoethanol (BME) NBT Phenol; chloroform 10 mM Phenylmethyl-sulfonyl fluoride (PMSF) Phosphate-buffered saline (PBS) Dissolve 214.46 g of magnesium acetate-4H20 in 800 ml of HaO. Adjust the volume to 1 liter with H20. Sterilize by filtration. Dissolve 203.3 g of MgCl3 ■ 6H20 in 800 ml of H30. Adjust the volume to 1 liter with H20. Dispense into aliquots and sterilize by auto-claving. Usually obtained as a 14.4 m solution. Store in a dark bottle at 4°C. Dissolve 0.5 g of nitro blue tetrazolium chloride, which is available from several manufacturers, in 10 ml of 70% dimethyl formám ide. Store at 4°C, Mix equal amounts of phenol and chloroform. Equilibrate the mixture by extracting several times with 0.1 m Tris-Cl (pH 7.6). Store the equilibrated mixture under an equal volume of 0.01 m Tris • CI (pH 7.6) at 4°C in dark glass bottles. Dissolve PMSF in isopropanol at a concentration of 1.74 mg/ml (10 mM). Divide the solution into aliquots and store at — 20°C. If necessary, stock solutions can be prepared in concentrations as high as 17.4 mg/ml (100 mM). Dissolve 8 g of NaCl, 0.2 g of KCl, 1.44 g of NařHP04, and 0.24 g of KH2P04 in 800 ml of distilled HsO. Adjust the pH to 7.4 with HCl. Add H20 to 1 liter. Dispense the solution into aliquots and sterilize them by autoclaving for 20 minutes at 15 lb/sq. in. on liquid cycle. Store at room temperature. MgCl2 is extremely hygroscopic. Buy small bottles (e.g., 100 g) and do not store opened bottles for long periods of time. Do not autoclave BME or solutions containing BME. Caution; Phenol is highly corrosive and can cause severe burns. Wear gloves, protective clothing, and safety glasses when handling phenol. All manipulations should be carried out in a chemical hood. Any areas of skin that come into contact with phenol should be rinsed with a large volume of water and washed with soap and water. Do not use ethanol. Caution: PMSF is extremely destructive to the mucous membranes of the respiratory tract, the eyes, and skin. It may be fatal if inhaled, swallowed, or absorbed through the skin. In case of contact, immediately flush eyes or skin with copious amounts of water. Discard con taminated clothing. PMSF is inactivated in aqueous solutions. The rate of inactivation increases with pH and is faster at 25°C than at 4°C. The half-life of a 20 fiui aqueous solution of PMSF is about 35 minutes at pH 8.0 (James 1978). This means that aqueous solutions of PMSF can be safely discarded after they have been rendered alkaline (pH>8.6) and stored for several hours at room temperature. 1 m Potassium acetate (pH 7.5) Potassium acetate (for alkaline lysis) 3 m Sodium acetate (pH 5.2 and pH 7.0) 5 m NaCl 10% Sodium dodecyl sulfate (SDS) (also called sodium lauryl sulfate) 20x SSC 20x SSPE Trichloroacetic acid (TCA) 100% solution 1 m Tris Dissolve 9.82 g of potassium acetate in 90 ml of pure H20 (Milli-Q or equivalent). Adjust the pH to 7.5 with 2 m acetic acid. Add pure H20 to 100 ml. Divide the solution into aliquots and store them at -20°C. To 60 ml of 5 m potassium acetate, add 11.5 ml of glacial acetic acid and 28.5 ml of H20. The resulting solution is 3 m with respect to potassium and 5 M with respect to acetate. Dissolve 408.1 g of sodium acetate * 3H20 in 800 ml of HĽ0. Adjust the pH to 5.2 with glacial acetic acid or adjust the pH to 7.0 with dilute acetic acid. Adjust the volume to 1 liter with H.,0 Dispense into aliquots and sterilize by autoclaving. Dissolve 292.2 g of NaCl in 800 ml of H20. Dis-and sterilize by auto- Adjust the volume to 1 liter with H20. pense into aliquots claving. Dissolve 100 g of electrophoresis-grade SDS in 900 ml of H20. Heat to 68°C to assist dissolution. Adjust the pH to 7.2 by adding a few drops of concentrated HCl. Adjust the volume to 1 liter with H20. Dispense into aliquots. Dissolve 175.3 g of NaCl and 88.2 g of sodium citrate in 800 ml of H20. Adjust the pH to 7.0 with a few drops of a 10 n solution of NaOH. Adjust the volume to 1 liter with H20. Dispense into aliquots. Sterilize by autoclaving. Dissolve 175.3 g of NaCl, 27.6 g of NaH2P04 • H20 and 7.4 g of EDTA in 800 ml of H20. Adjust the pH to 7.4 with NaOH (-6.5 ml of a 10 n solution). Adjust the volume to 1 liter with H20. Dispense into aliquots. Sterilize by autoclaving. To a bottle containing 500 g of TCA, add 227 ml of H20. The resulting solution will contain 100% (w/v) TCA. Dissolve 121.1 g of Tris base in 800 ml of H20, Adjust the pH to the desired value by adding concentrated HCl. pH HCl 7.4 70 ml 7.6 60 ml 8.0 42 ml Wear a mask when weighing SDS and wipe down the weighing area and balance after use because the fine crystals of SDS disperse easily. There is no need to sterilize 10% SDS. If the 1 m solution has a yellow color, discard it and obtain better quality Tris. Although many types of electrodes do not accurately measure the pH of Tris solutions, suitable electrodes can be obtained from most manufacturers. The pH of Tris solutions is temperature-dependent and decreases approximately 0.03 pH B,7 (continued) Solution Method of preparation Comments 1 m Tris (continued) Tris-buffered saline (TBS) (25 mM Tris) X-gal Allow the solution to cool to room temperature before making final adjustments to the pH. Adjust the volume of the solution to 1 liter with H20. Dispense into aliquots and sterilize by autoclaving. Dissolve 8 g of NaCl, 0.2 g of KCl, and 3 g of Tris base in 800 ml of distilled H20. Add 0.015 g of phenol red and adjust the pH to 7.4 with HCl. Add distilled H20 to 1 liter. Dispense the solution into aliquots and sterilize them by autoclaving for 20 minutes at 15 lb/sq. in. on liquid cycle. Store at room temperature. 5-Bromo-4-chloro-3-indolyl-/3-D-galactoside. Make a stock solution by dissolving X-gal in dimethylformamide to make a 20 mg/ml solution. Use a glass or polypropylene tube. The tube containing the solution should be wrapped in aluminum foil to prevent damage by light and should be stored at -20°C. It is not necessary to sterilize X-gal solutions by filtration. units for each 1°C increase in temperature. For example, a 0.05 m solution has pH values of 9.5, 8.9, and 8.6 at 5°C, 25°C, and 37°C, respectively. ENZYMES TABLE B.9 Proteolytic Ewtxymes Storage Concentration Reaction Stock solution temperature in reaction buffer Temperature Pretreatment Pronasea 20 mg/ml in H20 -20°C 1 mg/ml 0.01 MTris 37°C self-digestionb (pH7.8) 0.01 m EDTA 0.5% SDS Proteinase Kc 20mg/ml in H20 -20°C 50/xg/ml 0.01 MTris 37-56°C none required (pH 7.8) 0.005 M EDTA 0.5% SDS "Pronase is a mixture of serine and acid proteases isolated from Streptomyces griseus. b Self-digestion eliminates contamination with DNAase and RNAase. Self-digested pronase is prepared by dissolving powdered pronase in 10 mM Tris • CI (pH 7.5), 10 mM NaCl to a final concentration of 20 mg/ml and incubating for 1 hour at 37°C. Store the self-digested pronase in small aliquots at — 20°C in tightly capped tubes. ""Proteinase K is a highly active protease of the subtilisin type that is purified from the mold Tritirachium album Limber. The enzyme has two binding sites for Ca++, which lie some distance from the active site and are not directly involved in the catalytic mechanism. However, when Ca + + is removed from the enzyme, approximately 80% of the catalytic activity is lost because of long-range structural changes (Bajorath et al. 1989). Because the residual activity is usually sufficient to degrade proteins that commonly contaminate preparations of nucleic acids, digestion with proteinase K is usually carried out in the presence of EDTA (to inhibit the action of Mgf +-dependent nucleases). However, to digest highly resistant proteins such as keratin, it may be necessary to use a buffer containing 1 mM Ca++ and no EDTA. At the end of the digestion, the Ca+ + should be chelated by addition of EGTA (pH 8.0) to a final concentration of 2 mM before the nucleic acids are purified. ANTIBIOTICS TABLE A.l Antibiotic Solutions Working concentration Stock solution8 stringent relaxed concentration storage Plasmids plasmids Ampicillin 50mg/mlinH2O -20°C 20 /xg/ml 60 /xg/ml Carbenicillin 50mg/mlinH2O -20°C 20 /ig/ml 60 /xg/ml Chloramphenicol 34 mg/ml in ethanol -20°C 25 jLtg/ml 170 /xg/ml Kanamycin 10mg/mlinH2O -20°C 10 /ig/ml 50 jig/ml Streptomycin 10 mg/ml in H20 -20°C 10 /ig/ml 50 /xg/ml Tetracyclineb 5 mg/ml in ethanol -20°C 10 /xg/ml 50 /xg/ml aStock solutions of antibiotics dissolved in H20 should be sterilized by filtration through a 0.22-micron filter. Antibiotics dissolved in ethanol need not be sterilized. Store solutions in light-tight containers. bMagnesium ions are antagonists of tetracycline. Use media without magnesium salts (e.g., LB medium) for selection of bacteria resistant to tetracycline. COMMONLY USED BUFFERS TE pH 7.4 10 mM Tris • Cl (pH 7.4) 1 mM EDTA (pH 8.0) pH 7.6 10 dim Tris Cl (pH 7.6) 1 mM EDTA (pH £.0) pH 8.0 10 mM Tris-Cl (pH 8.0) 1 mM EDTA (pH 8.0) STE (also called TEN) 0.1 m NaCl 10 mM Tris • Cl (pH 8.0) 1 mM EDTA (pH 8.0) STET 0.1 m NaCl 10 mM Tris-Gl (pH 8.0) 1 mM EDTA (pH 8.0) 5% Triton X-100 TNT 10 mM Tris • Cl (pH 8.0) 150 mM NaCl 0.05% Tween 20