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Gentodenz
ref19-DENZ-50, ref19-DENZ-500
Density gradient medium
for cell separation.
Applications
for Gentodenz:
Separations based on density differences: fractionation of nucleic
acids, proteins, polysaccarides and nucleoproteins.Subcellular
organelles can be successfully isolated on gradients of Gentodenz under
either isotonic or mildly hypertonic conditions.Separation of intact
living cells.Useful in the isolation and purification of viruses and
bacteria.
Formation of gradients:
Gradients of Gentodenz can be generated as
follows:
1. Formed in situ by centrifugation
(self-forming gradients).
2. Layering solutions of the desired
concentration into an appropriate centrifuge tube and allowing the
solutions to diffuse. Using Gentodenz isotonic solution gradients can be
simply prepared in a hour.
3. Freezing and thawing.
4. Gradients mixers
Extended uses:
In
literature the product, the applications, the procedures are
described.Over more than 30 years the density gradient compound has been
sold by several commercial companies under different trade names.
Chemical info:
Structure: non-ionic tri-iodinated derivative of benzic acid with 3
aliphatic hydrophilic side chains.
Chemical name: 5- (N-2, 3-dihydroxypropylactamido)-2, 4, 6-tri-iodo-N,N’
–bis (2, 3 dihydroxypropyl) isophthalamide.
Purity: analytical grade
min 99.20 %
Molecular weight
821.14
Density
2.1 g/ml
Product description:
Gentodenz is non-ionc, non-toxic and is very water soluble. Solutions up
to 80 % (w/v) can be prepared. Aqueous solutions have a very high water
activity. Most particles will are fully hydrated in solutions of
Gentodenz and will band at a low density. Solutions of Gentodenz are
stable to heat and may be autoclaved, stability to autoclaving (enhanced
by the addition of small amounts of Tris and EDTA. Solutions of
Gentodenz are very resistant to bacterial degradation and Gentodenz is
not metabolized by mammalian cells.
The
concentration and density of solutions of Gentodenz can easily be
determined by measuring the refractive index.
The
relationship between concentration, refractive index (ŋ) and density is
linear and can be formulate:
Concentration, % (w/v)
= 607.75 ŋ – 810.13
Density (g/ml)
= 3.242 ŋ – 3.323
(Before using this equation the refractive index must be corrected for
the presence of buffer or salt in the gradient medium.)
Gentodenz is a non-particulate medium;therefore the distribution of
cells in a gradient can be determined using a haemocytometer, electronic
particle counter or by light-scattering measurements using a
spectrophotometer.
Gentodenz is also soluble in formamide and dimethyl formamide, for
non-aqueous denaturing gradients of Gentodenz.
Stability and storage:
Gentodenz in solid form is stable for a period of 5 years when stored at
room temperature and protected from light. Gentodenz in solution is
stable for 5 years provided that it is kept sterile and protected from
light. Prolonged exposure to direct sunkight leads to release of iodine
from the molecule. This effect is negligible when working with these
solutions on a day to day basis.
Isotonic Gradients
Gradients solution for the preparation of
essentially iso-osmotic Gentodenz gradients can be prepared using
an iso-osmotic solution of Gentodenz which contains
27.6% (w/v) Gentodenz (density=1.15 g/ml)
made up in buffered medium.
This solution may be diluted to desired
concentration by using a buffered diluent containing either sucrose or
NaCl as osmotic balancer.
The composition of these diluents is as
follows: 0.75 g NaCl or 7.45 g sucrose
Dissolved in 100 ml 5 mmol/Tris-HCl (pH
7.5) containing 3 mmol/l KCl and 0.3 mmol/l CaNa2 EDTA.
The relationship between density and
refractive index (ŋ) can be formulated:
NaCl diluent
Sucrose diluent
Density = 3.287 ŋ – 3.383
Density = 3.410 ŋ – 3.555
Compatibility with some
widely used assays:
Gentodenz does not interfere with the
orcinol and diphenylamine reactions for estimation of nucleic acids, nor
with the very sensitive dyebinding assays for protein and DNA.
Polysaccharides and sugars can be
determined in the presence of Gentodenz using the phenol/H2SO4 assay.
Fluorimetric assays of nucleic acid and
proteins can also be carried out in the presence of Gentodenz.
Gentodenz does not interfere with most
assays for the marker enzymes of subcellular components, also most
commercial scintillants are compatible with Gentodenz.
Removal of Gentodenz
from samples:
Gentodenz can be removed from samples by
dialysis, ultrafiltration and gel filtration. Cells, subcellular
organelles and other particulate matter can be separated from Gentodenz
by centrigugation without the risk of contaminating the pellet with
Gentodenz.
Gentodenz is readily soluble in both acidic
and ethanolic media. Thus in a number of cases samples can be isolated
free of Gentodenz by precipitating the sample with trichloroacetic or
ethanol.
Ordering
information:
Manufacturer
GENTAUR EUROPE
Avenue de l’Armée 68
B-1040 BRUSSELS
Phone: +32 16 58 90 45
Fax: +32 16 50 90 45
Info@gentaur.com
Product references :
50 gram ref19-DENZ-50
500 gram
ref19-DENZ-500 |