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51541

Sigma-Aldrich

Heparan sulfate sodium salt from bovine kidney

Synonym(s):

Heparitin sulfate sodium salt

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About This Item

CAS Number:
MDL number:
UNSPSC Code:
12352202

biological source

bovine kidney

impurities

~3% total nitrogen (N)

solubility

H2O: 1 mg/mL, clear, colorless

storage temp.

2-8°C

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Biochem/physiol Actions

Constituent of membrane-associated proteoglycans suggested to contribute to cell-cell adhesion

Other Notes

Antithrombotic activity in vivo[1]; Structure and function of heparan sulphate proteoglycans, review[2]
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Storage Class

13 - Non Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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Structure and function of heparan sulphate proteoglycans.
J T Gallagher et al.
The Biochemical journal, 236(2), 313-325 (1986-06-01)
Mahmoud A Omar et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 204, 702-707 (2018-07-10)
A new, specific, precise and very sensitive spectrofluorimetric methodology has been established and approved for determination of Fenoterol hydrobromide (FEN) in its pharmaceutical forms and spiked plasma. The strategy utilized the phenolic nature of FEN and its capacity to undergo
P Bianchini et al.
Thrombosis research, 40(5), 597-607 (1985-12-01)
The anticoagulant (U.S.P., APTT; "in vitro" and "in vivo") antithrombotic (aXa; Yin and Wessler and chromogenic), antilipemic (LPL) activities of heparin, heparin fractions and fragments, heparinoids, heparan sulfate and other sulfated glycosaminoglycans were compared with the activities of these compounds
U Benelli et al.
Experimental eye research, 67(2), 133-142 (1998-09-12)
The purpose of this study was to evaluate the inhibitory activity of the heparan sulfate suleparoide on vascular cell growth in vitro and angiogenesis in vivo. Human HUV-EC-C endothelial cell proliferation and microvessel sprouting from cultured rat aortic rings were
Comparative pharmacologic profile of a glycosaminoglycan mixture, Sulodexide, and a chemically modified heparin derivative, Suleparoide.
D D Callas et al.
Seminars in thrombosis and hemostasis, 19 Suppl 1, 49-57 (1993-01-01)

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