Animal Enteritis modeling reagent-dextran sulfate sodium (DSS)
- The pathological changes of the DSS-induced UC model are similar to those of human UC;
- This model can be applied to both the acute and chronic phases of UC research, allowing experiments to be conducted completely;
- Simple, economical and easy to produce.
Description: Dextran sulfate is a polyanionic derivative of dextran, formed by the esterification reaction of dextran and chlorosulfonic acid. The sulfur content is about 17%, which is equivalent to an average of 1.9 sulfate groups in each glucose residual sugar of the dextran molecule.
Solubility: soluble in water (100mg/ml - clear or slightly hazy yellow solution, high molecular weight products are not as soluble in water as low molecular weight products). Before sterilization, the aqueous solution should be formulated into a buffer system (such as sodium bicarbonate) to prevent degradation.
When the solution contains 10% dextran sulfate, the re-annealing rate of the DNA chain increases approximately 10 times. This phenomenon further expands the hybridization rate between single-stranded or double-stranded probes and DNA/RNA fixed on the membrane. Not only that, adding 10% dextran sulfate may increase the hybridization rate of randomly cleaved double-stranded DNA probes and immobilized nucleic acids by up to 100 times.
- Enhancement and suppression of humoral immunity;
- Polyclonal activation of B lymphocytes can even stimulate immature B cells;
- In the thymocyte reaction, it promotes conversion into lectin;
- Inhibit blood coagulation and platelet aggregation
- Enhance fibrinolytic activity;
- Enhance/suppress cell-mediated immune response;
Item number
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product name
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average molecular weight
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DCJ0018A
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Dextran sulfate sodium (DSS)
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Mw 5,000
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DCJ1606A
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Dextran sulfate sodium (DSS)
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Mw 40,000
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DCJ0105A
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Dextran sulfate sodium (DSS)
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Mw 36,000~50,000
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Use method for reference
Mice were given distilled water containing 50g/L dextran sulfate (dextran sulfate sodium) 5000 or 40000 to drink freely for 7 days, and symptoms of acute enteritis such as weight loss, diarrhea, and bloody stools appeared. HE staining of pathological sections revealed diseased colons of mice. The glandular structure was disordered, and the mucosa and submucosal infiltration of mononuclear cells and multinucleated cells was observed. The expression of GSH in the diseased intestinal segment tissue of the DSS group was significantly lower than that of the control group (2±0.6 vs 3.14±1.0, t = 3.95, P = 0.01<0.05). IL-4 secreted by the diseased colon was significantly increased (38.7±4.7 vs 28.7±6.7, t = 3.16, P = 0.009<0.01), and IFN-g was slightly decreased (P>0.05).Source: "The role of GSH in DSS-induced experimental enteritis in mice"