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BioUltra Reagents

Density Gradient

Introduction
References
Product List


To meet highest demands for quality, we offer a wide range of BioUltra Reagents for density gradient centrifugation.


Introduction

Criteria for an ideal density gradient centrifugation medium are:

  • the additive must form a solution within the required density range
  • the additive must not interfere with, or damage, the sample
  • the solvent must be compatible with the sample
  • the solution must have a refractive index within the pratical range, as well as a low viscosity
  • the additive must be easily removable from the sample.

The additives for density gradient centrifugation can be divided into four main categories:

  1. Salts of Alkali Metals

    These solutions fulfill most of the above requirements. However, due to the high ionic strength, hydrogen bonding within biological macromolecules (protein, nucleic acid - protein complexes) is impaired by a chaotropic effect. Therefore these salts are mainly used for DNA and RNA separations. Cesium chloride is used most frequently. Other useful salts include sodium iodide, sodium bromide, cesium sulfate and cesium acetate. Potassium tartrate has been used to separate viruses from host cells.
    It should be kept in mind that the density of the sample is highly dependent on the hydration of the macromolecule, which in turn depends to a large extent on the dehydration power of the salt solution.


  2. Neutral, Water-Soluble Molecules

    In this class of compounds sucrose is most widely used. It has a useful density range of up to 1.29. This range can be increased to 1.37 by addition of glucose or by dissolving sucrose in D2O. Sucrose has very little effect on macromolecules, but affects enzyme activity. Due to its high osmotic pressure, sucrose solution dehydrates cells and their organellae very efficiently. Glycerol solutions are the preferred media for the separation of enzymes because they do not affect enzyme activity. They exhibit a high viscosity, requiring prolonged centrifugation times. More importantly however, glycerol penetrates biological membranes.

     

  3. Hydrophilic Macromolecules

    Dextran gradients have been used for the separation of microsomes. Separations achieved with dextrans show similar results to those obtained by using synthetic sucrose/ epichlorohydrin co-polymers. In some cases bovine serum albumin has been applied, but the preparation of an appropriate solution is very difficult.

     

  4. Synthetic Molecules

    These additives are the sodium or methyl glucamine salt of triiodobenzoic acid and of metrizoic acid. It should be kept in mind that the parent acid of these salts may precipitate on adjusting the pH to acidic values. Metrizamide, a covalently bonded compound of glycosamine and metrizoic acid is most widely used. This additive forms solutions of relatively low viscosity. These solutions are stable over a wide range of pH and ionic strength, and show practically no interference with the analytes.


    References:

    R. Hinton M. Dobrota, in: Laboratory Techniques in Biochemistry and Molecular Biology (TW.Work, E.Work, ebs.), North Holland Publ.Comp., Amsterdam (1976).


    Nomogram for Determination of g-number x


    Formula(1) describes the dependence of the cetrifugal field g (in g-numbers x) with revolutions per min, n, and with distance, r (in centimeters), from the midpoint of the rotor to the point at which the field is determined.

    xg= 1118 x 10-8 x r x n2 (1)
    (g= gravity accelaration of earth)



    Properties of Aqueous Solutions of 84097 and 84099 Sucrose BioUltra

    (Density, Refractive Index and Viscosity vs w/w-% sucrose)


    For explicit data on the viscosity and refractive index of aqueous solutions at various temperatures: D. Ridge, in: Centrifugal Separations in Molecular and Cell Biology (D. D. Birnie, D.Rickwood, eds.), p.33, Butterworth, London and Boston (1978) Barber, Natl. Cancer Inst. Monographs 2;, 219 (1966)

    Density of Gradient Centrifugation Media and their Useful Range calculated from n25 D

        p lower p upper Density (r ) at 25°C

    CsCI 1.0 1.9 1.1584-10.2219 n25D + 7.5806 n25D)2
    Cs2SO4 1.15 1.8 0.9945 + 11.1066 (n25D-n0) - 26.4460 (n25D-n0
    CsBr 1.05 1.5 2.7798 - 12.2102 n25D + 8.1615 (n25D)2
    Metrizamide 1.05 1.42 3.350 n20D- 3.462 (20°C)
    NaCI 1.0 1.2 4.23061 n25D-4.64125
    NaBr 1.1 1.4 6.4786 n25D - 7.6431
    RbCI 1.08 1.35 21.7661 - 39.2834 n25D + 17.7843 (n25D)2
    Sucrose 1.0 1.35 See below, equation (2)


    Calculation of Density of Sucrose between 0° and 30°C [1]


    p (T) = (B1+ B2T+ B3T2) + (B4 + B5T+ B6T2)Y + (B7 + B8T + B9T2)Y2 (2)


    T = Temperature °C
    Y = weight fraction of sucrose in solution
    B1-9 = constants
    B1: 1.00037
    B2: 3.96805x10-5
    B3: -5.85133 x10-6
    B4: 0.389824
    B5 -1.05789x10-3
    B6: 1.23928x10-5
    B7: 0.170976
    B8: 4.75301 x10-4
    B9: -8.92397x10-6

    Tables of density and refractive index vs w/w-% solutions of sucrose and CsCI can be found in [2]



    References

    1. Barber, Natl. Cancer Inst. Monographs 21, 219 (1966).
    2. R.M.C. Dawson et al., Data for Biochemical Research, Clarendon Press, Oxford (1986)