Phosphate buffer solution

Biological activity (BA) was chosen as such parameter. The BA determined using a system and a technique for a class of natural polyphenolic bonds nicotinamide adenine dinucleotide restored (NAD H ) - ferricyanide (KjFe(CN)g) in a phosphates buffer solution. 

The working conditions of the immunosensor (enzyme and antigen concentrations, dilutions of the antibodies, pH of the buffer solution) were found. The cholinesterase immobilized demonstrated the maximum catalytic activity in phosphate buffer solution with pH 8.0. The analytical chai acteristics of the sensor - the interval of the working concentrations and detection limit - have been obtained. The proposed approach of immunoassay made possible to detect 5T0 mg/ml of the bacterial antigen. 

Distribution of benzodiazepines in I-octanol - water system was investigated by a direct shake flask method at the presence of the compounds used in HPLC mobile phases the phosphate buffer with pH 6,87 (substances (I) - (II)), acetic and phosphate buffer, perchloric acid at pH 3 (substances (III) - (VI)). Concentrations of substances in an aqueous phase after distribution controlled by HPLC (chromatograph Hewlett Packard, column Nucleosil 100-5 C, mobile phase acetonitrile - phosphate buffer solution with pH 2,5, 30 70 (v/v)). 

Note The pre- and post-treatment of the chromatograms with the basic tri-ethylamine solution, which can be replaced by an alcoholic solution of sodium hydroxide [1,4] or a phosphate buffer solution pH = 8.0 (c = 0.2 mol/1) [5], serves to stabilize the fluorescence of the amino derivatives [2]. A final spraying with methanolic hydrochloric acid (chci = 5 mol/1) or 70% perchloric acid renders the detection reaction highly specific for histamine [4] and for catecholamines and indolamines [5]. 

FIGURE l.l Hydrophobic interaction and reversed-phase chromatography (HIC-RPC). Two-dimensional separation of proteins and alkylbenzenes in consecutive HIC and RPC modes. Column 100 X 8 mm i.d. HIC mobile phase, gradient decreasing from 1.7 to 0 mol/liter ammonium sulfate in 0.02 mol/liter phosphate buffer solution (pH 7) in 15 min. RPC mobile phase, 0.02 mol/liter phosphate buffer solution (pH 7) acetonitrile (65 35 vol/vol) flow rate, I ml/min UV detection 254 nm. Peaks (I) cytochrome c, (2) ribonuclease A, (3) conalbumin, (4) lysozyme, (5) soybean trypsin inhibitor, (6) benzene, (7) toluene, (8) ethylbenzene, (9) propylbenzene, (10) butylbenzene, and (II) amylbenzene. [Reprinted from J. M. J. Frechet (1996). Pore-size specific modification as an approach to a separation media for single-column, two-dimensional HPLC, Am. Lab. 28, 18, p. 31. Copyright 1996 by International Scientific Communications, Inc.. Shelton, CT.]... 

An amount of enzyme preparation equivalent to 900 mg of wet cells was made up to 25 ml with the above potassium phosphate buffer solution. 150 mg (1.15 mmol) of 5-fluorouracil and 1.0 gram of thymidine (4.12 mmol) were dissolved in 15 ml of the above potassium phosphate buffer solution. The mixture was incubated at 37°C for 18 hours. After this time, enzyme action was stopped by the addition of four volumes of acetone and one volume of peroxide-free diethyl ether. The precipitated solids were removed by filtration, and the filtrate was evaporated under nitrogen at reduced pressure until substantially all volatile organic solvent had been removed. About 20 ml of aqueous solution, essentially free of organic solvent, remained. This solution was diluted to 100 ml with distilled water. 

Do Due, H., Meyer R. M. and Tissot, P. Electrochemical Behaviour of SngHg (gamma-2) and Dental Amalgam in a Phosphate Buffer Solution , Electrochimica Acta, 25, 851-6 (1980)... 

When the electrode is placed in an aqueous solution of glucose which has been suitably diluted with a phosphate buffer solution (pH 7.3), solution passes through the outer membrane into the enzyme where hydroxen peroxide is produced. Hydrogen peroxide can diffuse through the inner membrane which, however, is impermeable to other components of the solution. The electrode vessel contains phosphate buffer, a platinum wire and a silver wire which act as electrodes. A potential of 0.7 volts is applied to the electrodes (the apparatus shown in Fig. 16.17 is suitable) with the platinum wire as anode. At this electrode the reaction H202->02 + 2H+ +2e takes place, and the oxygen produced is reduced at the silver cathode ... 

Fig. 6.1.7 Effect of pH on the initial light intensity and total light of Latia bioluminescence reaction in the presence of the purple protein, in 50 mM sodium phosphate buffer solutions having various pH values at 25°C (Shimomura et al., 1966b).

Fig. 7.1.6 Influence of pH and temperature on the luminescence of Cbaetopterus photoprotein elicited by old dioxane and Fe2+ in 20 mM phosphate buffer. Left panel the effect of pH in phosphate buffer solutions of various pH values, at 22°C. Right panel the effect of temperature at pH 7.2. Luminescence was initiated by the injection of Fe2+. The time lag of the light emission after the Fe2+ injection was also shown in the right panel. From Shimomura and Johnson, 1966.

Monitor DO level and control pH at 6.7-7 by using 0.2 M phosphate buffer solution. 

Figure 5. Thickness of the anodic passivating film formed on iron at various potentials.6 9 Lbl and Lr, are the thicknesses of the barrier layer and the precipitated layer, respectively. Temperature is 25°C. , in a 150 mol m 3 phosphate buffer solution at pH 1.85 O, in a 300 mol m 3 borate buffer solution at pH 8.2. (From N. Sato, K. Kudo, and T. Noda, Z Phys. Chem. N. F. 98,271,1975, Fig. 5, reproduced with permission and N. Sato, K. Kudo, and R. Nishimura, / Elec-trochem. Soc, 123,1420,1976, Fig. 1. Reproduced with permission of the Electrochemical Society, Inc.)...

Spray solution 2 Dissolve 4 g sodium dithionite (Na2S204> in 100 ml 0.5 mol phosphate buffer solution (pH 6.5). This solution is only stable for about 1 h, so it should always be made up fresh. 

FIGURE 1 Rate of polyanhydride degradation versus time. PCPP and SA copolymers were formulated into 1.4-cm-diameter disks 1 mm thick by compression molding, and placed into a 0.1 M pH 7.4 phosphate buffer solution at 37°C. The cumulative percentage of the polymer which degraded was measured by absorbance at 250 nm. 

C18-0120. You are doing undergraduate research for a biology professor. Your first assignment is to prepare a pH =7.50 phosphate buffer solution to be used in the isolation of DNA from a cell culture. The buffer must have a total concentration of 0.500 M. On the shelf you find the following chemicals solid NaOH concentrated HCl (12.0 M) concentrated H3 PO4 (14.7 M) KH2 PO4 and K2 HPO4. Write a quantitative detailed set of instmctions that describe how you would prepare 1.5 L of the buffer solution. 

Adiponitrile is readily hydrogenated catalytically to hexamethylenediamine, which is an important starting material for the prodnction of nylons and other plastics. The electrochemical production of adiponitrile was started in the United States in 1965 at present its volume is about 200 kilotons per year. The reaction occurs at lead or cadmium cathodes with current densities of np to 200 mA/cm in phosphate buffer solutions of pH 8.5 to 9. Salts of tetrabntylammonium [N(C4H9)4] are added to the solution this cation is specihcally adsorbed on the cathode and displaces water molecules from the first solution layer at the snrface. Therefore, the concentration of proton donors is drastically rednced in the reaction zone, and the reaction follows the scheme of (15.36) rather than that of (15.35), which wonld yield propi-onitrile. 

M Phosphate buffer solution (pH 7.4), guaranteed reagent 0.2 M Acetate buffer solution (pH 4), guaranteed reagent... 

Transfer the residue prepared as in Section 6.1.1 into a 300-nL separatory funnel with 25 mL of phosphate buffer solution (0.1 M, pH 7.4). Add 10 mL of saturated aqueous sodium chloride and 50 mL of 0.5 M sodium hydrogen carbonate to the funnel and shake the funnel vigorously for 1 min. Add 70 mL of ethyl acetate to wash the aqueous layer to the funnel, shake, separate, and discard the ethyl acetate layer. Repeat this extraction procedure three times. Add 2 mL of phosphoric acid and 20 mL of an acetate buffer solution (0.1 M, pH 4) to the aqueous layer and extract the mixmre with 50 mL of ethyl acetate three times. Combine the extracts and filter into a 500-mL round-bottom flask through 60 g of anhydrous sodium sulfate supported by a plug of cotton wool in a funnel. Concentrate the filtrate to dryness under reduced pressure. 

Chloroform, sodium chloride, anhydrous sodium sulfate, sulfuric acid (97%), hydrochloric acid (36%), sodium bicarbonate, trifluoroacetic acid, tris(hydro-xymethyl)aminomethane (Tris), special grade Water, high-performance liquid chromatography grade 0.1 M Phosphate buffer solution (pH 7.0)... 

Extract the chloroform-methanol layer from the strawberry, rice grain, barley grain and rice straw samples twice with 30 mL of 0.1 M phosphate buffer solution (pH 7.0). Since an emulsion is formed, the first extraction should be conducted with very gentle shaking. Centrifuge the extract at 2500 rpm for 10 min, when an emulsion is formed. Discard the chloroform-methanol layer. 

Cleanup procedure for IC-0. Dissolve the residue with 10 mL of pH 5 phosphate buffer solution and apply the solution to the top the Sep-Pak Cig Env. column pretreated with 10 mL each of methanol and distilled water. Discard the passed solution and elute IC-0 with 15 mL of a second buffer solution. Add 35 mL of distilled water and adjust the pH of solution to 1.5 with hydrochloric acid. Extract the solution with three portions of 50 mL of diethyl ether. Combine the diethyl ether extracts and dry over anhydrous sodium sulfate. Concentrate to dryness on a water-bath at ca 40 °C... 

Transfer the concentrate into a 200-mL separatory funnel with 40 mL of n-hexane and 30 mL of 1 N HCl. After shaking for 5 min, drain the aqueous layer into another 200-mL separatory funnel and extract the n-hexane layer further with 30 mL of 1 N HCl. Combine the aqueous layers and neutralize to pH 7 with 6mL of 10 M NaOH and 50 mL of IM phosphate buffer solution. Extract buprofezin and p-OH-buprofezin in the neutralized aqueous solution with 50 mL of n-hexane twice. 

In a typical test 750 mg of catalyst was added to a continuous stirred tank reactor containing the nitrate ions in 1 L of phosphate buffer solution. This suspension contained 85% H3PO4 (331 g), NaNOs (198 g), NaOH (84g), and Ge02 dissolved in water and was stirred under a H2 flow of 150 L/h. The amonnt of hyam formed and selectivity after 90 min at 30°C were measured by titration [2-3]. Catalysts A and C were also chosen for stndying the effect of Pd loading and Pt addition. 

Aromatic diazo compounds can be reduced in water via a radical process (Scheme 11.5).108 The reduction mechanism of arenediazo-nium salts by hydroquinone was studied in detail.109 Arenediazonium tetrafluoroborate salts undergo facile electron-transfer reactions with hydroquinone in aqueous phosphate-buffered solution containing the hydrogen donor solvent acetonitrile. Reaction rates are first order in a... 

Eight samples from each set (A and D) were split into two groups, one incubated in 0.15 M phosphate buffered solution (PBS) and the other in PBS containing 0.1% of the phase transfer catalyst, tricapryl methyl ammonium chloride (Aldrich Aliquot 336) (PBS, catalyzed), both at pH 7.4. The samples were suspended in centrifuge tubes with 10 mL of incubation solution by nylon string and the tubes were placed in a shaker bath at a constant temperature of 37°C. Periodically, the samples were taken out of the tubes, placed on lint free paper towels, allowed to dry for exactly one hour, weighed and placed in fresh incubation media. The total time of the study was 48 weeks (330 days). 

The native SGPA crystals have been prepared from a phosphate buffered solution at a pH of 4.3 (cf. Ref. 118)... 

Mann and Mitchell [58] described a simple colorimetric method for estimation of (-D)-penicillamine in plasma. Blood containing 2-50 pg of penicillamine was mixed with 0.1 M EDTA solution in tromethamine buffer solution. 0.1 mL of this solution was adjusted to pH 7.4 and centrifuged. To a portion of the plasma was added 3 M HCL, the mixture was freeze-dried, and a suspension of the residue in ethanol was centrifuged. The supernatant liquid was mixed with tromethamine buffer solution (pH 8.2) and 10 mM 5,5 -dithiobis-(2-nitrobenzoic acid) in phosphate buffer solution (pH 7.0), the mixture was shaken with ethyl ether, and the absorbance of the separated aqueous layer was measured at 412 nm. The mean recovery was 60% (four determinations), and the calibration graph was linear for the cited range. 

Figure 3.91 Cyclic voltammograms of 1 mM fa) SSBipy and (b) PySH in a phosphate buffer solution with 0.1 M NaC104 (pH 7.0) at a SERS-activated gold electrode. Scan rate 50mVs , ...

After heating process, wash slides with phosphate buffer solution followed by IHC staining procedure. 

Hestrin, Avineri-Shapiro and Aschner9 report that levan formation by means of B. subtilis is greater if cultural products other than levan are continually removed by dilution or dialysis. The organism was inoculated into a phosphate-buffered solution contained in a cellophane bag suspended in a large volume of sucrose peptone solution. 

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