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75027

Sigma-Aldrich

Dextran sulfate sodium salt

Synonym(s):

Sodium Dextran Sulfate

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About This Item

UNSPSC Code:
12352201
NACRES:
NA.25

form

powder

Quality Level

mol wt

Mr ~4000

impurities

3-6% (sulfur content)

loss

≤10% loss on drying

color

colorless

useful pH range

6.0-8.0 (10 g/L)

solubility

H2O: 100 mg/mL, clear, colorless to faintly greenish-yellow

storage temp.

room temp

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General description

Dextran is a polymer of anhydroglucose. It is composed of approximately 95% alpha-D-(166) linkages. The remaining (163) linkages account for the branching of dextran.

Application

Dextran sulfate is routinely used for the selective precipitation of lipoproteins, probe hybridization membrane-immobilized DNA, the release of DNA from DNA-histone complexes, and the inhibition of RNA binding to ribosomes.

Biochem/physiol Actions

Dextran sulfate was able to inhibit the binding of platelet factor 4 to S aureus bacterial surface in a dose dependent manner.

Other Notes

To gain a comprehensive understanding of our extensive range of Dextrans for your research, we encourage you to visit our Carbohydrates Category page.

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Krystin Krauel et al.
Blood, 117(4), 1370-1378 (2010-10-21)
A clinically important adverse drug reaction, heparin-induced thrombocytopenia (HIT), is induced by antibodies specific for complexes of the chemokine platelet factor 4 (PF4) and the polyanion heparin. Even heparin-naive patients can generate anti-PF4/heparin IgG as early as day 4 of
Johannes Mehringer et al.
Physical chemistry chemical physics : PCCP, 23(2), 1381-1391 (2021-01-05)
Amphiphilic molecules (e.g. hydrotropes) that enhance the solubility of hydrophobic compounds in water are often charged. As a result, such compounds also show specific ion effects. These effects can either strengthen or weaken the solubilisation power of amphiphilic molecules, depending

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