Sucrose solution containing

CORRECTION TABLE FOR TOTAL SOLUBLE SOLIDS DETERMINED BY MEANS OF THE REFRACTOMETER IN SUCROSE SOLUTIONS CONTAINING CITRIC ACID (2)... 

Etanercept is available as a preservative-free powder for reconstitution or as a solution in prefilled syringes. The powder should be reconstituted in bacteriostatic water, containing 0.9% benzyl alcohol, to a final concentration of etanercept of 25 mg/mL. The prefilled syringes contain 25 mg or 50 mg etanercept in a 1% sucrose solution containing sodium phosphate, sodium chloride and l-arginine. Both preparations are administered by subcutaneous injection. 

Kokini, J. L., Bistany, K., Poole, M., and Stier, E. 1982. Use of mass transfer theory to predict viscosity-sweetness interactions of fructose and sucrose solutions containing tomato solids. J. Texture Stud. 13 187-200. 

Nonelectrolytes in aqueous solution Many molecular compounds dissolve in solvents but do not ionize. Such solutions do not conduct an electric current, and the solutes are called nonelectrolytes. Sucrose is an example of a nonelectrolyte. A Im sucrose solution contains only one mole of sucrose particles. Figure 15-16 compares the conductivity of a solution containing an electrolyte solute with one containing a nonelectrolyte solute. Which compound would have the greater effect on colligative properties, sodium chloride or sucrose ... 

Cameron (S) and others (5, page 48) have found that sweetness is not a linear function of concentration, and that the relative sweetness of different sugars varies with the concentrations at which they are compared. Sweetness is influenced by temperature, pH, and the presence of other substances which need not themselves be sweeteners. For example, a 5% sucrose solution containing 2% urea was found to be equal in sweetness to a 3.1% sucrose solution. Thus, sweetness had been reduced 38% by the presence of urea. 

Determination of Lipid Peroxidation in Mitochondria and Microsomes. Rats were killed by decapitation after fa.sting for 24 hours and their liver tissue was quickly removed. Microsomal and mitochondria fractions were isolated from the liver tissue by the method of Oda (9J. The liver tissues were cut into small slices in 0.25 M sucrose containing 3 mM Tris-MCI and 0,1 mM EDTA (pH 7.4) at 4°C, and then small slices of liver tissues were homogeniaed with nine times (the amount by weight) 0.25 M sucrose solution containing 3 mM Tris-HCl and 0.1 mM EDTA (pH... 

Fig. 1. Treatment of free mRNP with 0.5 M KCl. Mouse plasmacytoma free mRNP (150 ig protein) were layered on 10-30% (w/w) sucrose gradients over a 50% (w/w) sucrose cushion and centrifuged 15 hr at 39,000 rpm, 4°C in a Beckman SW 41 rotor. All sucrose solutions contained 10 mM TEACl (pH 7.4), 2 mM MgCl2, 5 mM fi-mercaptoethanol and 0.1 mM PMSF. A, Aliquots were removed from each fraction of the gradients and tested for poly(ADP-ribose) polymerase activity as described in (6). Free mRNP treated with 0.05 M KCl (A), or with 0.5 M KCl (A). B, free mRNP were p2p]ADP-ribosylated with 1 iM NAD prior to analysis on 10-30% sucrose gradients. Protein aliquots from each fraction were precipitated with TCA and the radioactivity of the precipitates was measured. Free mRNP treated with 0.05 M KCl ( ), or with 0.5 M KC1( ).

Ryoo et al. [62] impregnated the pores of MCM-48 with a sucrose solution containing sulfnric acid, followed by carbonization at 900°C and removal of the silica framework to produce an OMC sample designed as CMK-1. Other carbon precursors, including glucose, xylose, FA, and phenolic resin, can also be used. The surface area of CMK-1 was reported to be in the range of 1300-1800 mVg... 

Calculate the mass percent of a sucrose solution containing 11.3 g of sucrose and 412.1 mL of water. (Assume that the density of water is 1.00 g/mL.)... 

The chloroplasts and chromoplasts were isolated after immersion of fruit pericarp in sucrose solution containing p-mecraptoethanol, EDTA, Tris and ascorbic acid. 

Aliquots of Sepharose 4B (0.5 ml settled volume) or Sepharose 4B coupled to anti-cathepsin M, or to a monoclonal antibody directed against human platelet glycoprotein, as indicated, were washed with 0.25 M sucrose containing 10 mM sodium borate, pH 7.4. The resins were then suspended in 2 ml of the same buflFered sucrose solution containing 1 mg/ml of bovine serum albumin and 100/tl of the heavy particle fraction (0.99 mg/ml of protein). The mixtures were rotated end-over-end for 30 minutes at 5°C and the resins collected by free sedimentation and washed six times with the same buffered isotonic sucrose mixture. The washed gels were suspended in 0.5 ml of 0.5% Triton X-100 and after 10 minutes at room temperature the supernatant solutions were assayed for cathepsin C activity. From Pontre-moli et al. (31) reproduced with permission. 

Various extraction liquids are recommended by the FDA including distilled water, 3% aqueous acetic acid, 3% aqueous sodium bicarbonate, 3% aqueous sodium chloride, aqueous ethyl alcohol of the appropriate concentration, 20% sucrose solution containing 1% citric acid adjusted to pH 3.5 (aqueous extractants) and a liquid food fat, e.g., olive oil, vegetable oil, heptane and diethyl ether (fatty extractants). 

Testis cells of the rainbow trout were homogenized in 2.2 M sucrose solution containing 0.05 M sodium glycerophosphate at pH 7.9 The mixture was filtered through layers of gauze and centrifuged at 14,000 x g for 20 min. The treatment was then repeated, the sediment was blended with 0.25 M sucrose solution and centrifuged. The purified nuclear fraction thus obtained was used as material for further preparation of basic and acidic nuclear proteins (cf. Chap. III. C. 2. c)y). 

FIG. D-7 Mass loss of water from (a) 5% w/v sucrose solution, (d) 5% w/v sucrose solution containing 5% w/v TBA. Drying temperature -35 °C in the microbalance. (Source Kasraian, K., DeLuca, P., Pharmaceutical Research, Vol. 12, No. 4,1995 permitted by the Plenum Publishing Corporation.)... 

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