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Supplier: Thermo Scientific Chemicals
Description: D-Glucosamine Sulfate, Purity: 98%, CAS Number: 29031-19-4, Molecular Formula: C6H13NO5.H2SO4, Form: Powder, Synonym: Chitosamine sulfate, 2-Amino-2-deoxy-D-glucose sulfate, Size: 25g
Supplier: Spectrum Chemicals
Description: Glucosamine Sulfate Potassium Chloride, Dietary Supplement, USP. 
Catalog Number: (103222-544)
Supplier: Novus Biologicals
Description: Heparan Sulfate Glucosamine 3-O-Sulfotransferase 3 Antibody, Polyclonal, Host: Sheep, Species: Human, IgG, Chinese hamster ovary cell line CHO-derived human Heparan Sulfate Glucosamine 3-O-Sulfotransferase, Size: 100UG


Catalog Number: (76703-160)
Supplier: AFG BIOSCIENCE LLC
Description: Mouse Heparan Sulfate glucosamine 3-O-sulfotransferase 2(HS3ST2) ELISA Kit


Catalog Number: (103222-546)
Supplier: Novus Biologicals
Description: Heparan Sulfate Glucosamine 3-O-Sulfotransferase 3 Antibody, Polyclonal, Host: Sheep, Species: Human, Immunogen: Chinese hamster ovary cell line CHO-derived human Heparan Sulfate Glucosamine 3-O-Sulfotransferase, Size: 25UG


Catalog Number: (76700-172)
Supplier: AFG BIOSCIENCE LLC
Description: Human Heparan Sulfate Glucosamine 3-O-Sulfotransferase 4(HS3ST4) ELISA Kit


Catalog Number: (76705-630)
Supplier: AFG BIOSCIENCE LLC
Description: Human Heparan Sulfate Glucosamine 3-O-Sulfotransferase 1(HS3ST1) ELISA Kit


Catalog Number: (76714-118)
Supplier: AFG BIOSCIENCE LLC
Description: Human Heparan Sulfate Glucosamine 3-O-Sulfotransferase 2(HS3ST2) ELISA Kit


Catalog Number: (89424-258)
Supplier: Genetex
Description: Rabbit Polyclonal antibody to HS3ST2 (heparan sulfate (glucosamine) 3-O-sulfotransferase 2)


Catalog Number: (10299-022)
Supplier: Bioss
Description: GNS is a 552 amino acid lysosomal enzyme that hydrolyzes the 6-sulfate groups of the N-acetyl-D-glucosamine 6-sulfate units of keratan sulfate and heparan sulfate. A member of the sulfatase family, GNS assists in the catabolism of heparin, and binds calcium as a cofactor. GNS deficiency results in an autosomal recessive lysosomal storage disorder known as mucopolysaccharidosis type IIID (Sanfilippo D syndrome), which is characterized by mild somatic disease and severe degeneration of the central nervous system. Subject to post-translational internal peptidase cleavage, GNS is encoded by a gene mapping to human chromosome 12q14.2 and mouse chromosome 10 D2.


Supplier: MP Biomedicals
Description: Heparin is a polymer classified as a mucopolysaccharide or a glycosoaminoglycan. It is biosynthesized and stored in mast cells of various mammalian tissues, particularly liver, lung and mucosa. It is made up of repeated disaccharide units consisting of 1,4-linked L-iduronic acid and D-glucosamine. The iduronic acid residues are O-sulfated at position 2, and the glucosamine residues are N-sulfated and O-sulfated at position 6. The repeated block can be interrupted or extended by residues of beta-D-glucuronic acid and 6-O-sulfated N-acetyl-alpha-D-glucosamine.

Catalog Number: (10298-888)
Supplier: Bioss
Description: GNS is a 552 amino acid lysosomal enzyme that hydrolyzes the 6-sulfate groups of the N-acetyl-D-glucosamine 6-sulfate units of keratan sulfate and heparan sulfate. A member of the sulfatase family, GNS assists in the catabolism of heparin, and binds calcium as a cofactor. GNS deficiency results in an autosomal recessive lysosomal storage disorder known as mucopolysaccharidosis type IIID (Sanfilippo D syndrome), which is characterized by mild somatic disease and severe degeneration of the central nervous system. Subject to post-translational internal peptidase cleavage, GNS is encoded by a gene mapping to human chromosome 12q14.2 and mouse chromosome 10 D2.


Catalog Number: (76120-524)
Supplier: Bioss
Description: Essential bifunctional enzyme that catalyzes both the N-deacetylation and the N-sulfation of glucosamine (GlcNAc) of the glycosaminoglycan in heparan sulfate. Modifies the GlcNAc-GlcA dissacharide repeating sugar backbone to make N-sulfated heparosan, a prerequisite substrate for later modifications in heparin biosynthesis. Plays a role in determining the extent and pattern of sulfation of heparan sulfate. Compared to other NDST enzymes, its presence is absolutely required. Participates in biosynthesis of heparan sulfate that can ultimately serve as L-selectin ligands, thereby playing a role in inflammatory response.


Catalog Number: (10298-884)
Supplier: Bioss
Description: GNS is a 552 amino acid lysosomal enzyme that hydrolyzes the 6-sulfate groups of the N-acetyl-D-glucosamine 6-sulfate units of keratan sulfate and heparan sulfate. A member of the sulfatase family, GNS assists in the catabolism of heparin, and binds calcium as a cofactor. GNS deficiency results in an autosomal recessive lysosomal storage disorder known as mucopolysaccharidosis type IIID (Sanfilippo D syndrome), which is characterized by mild somatic disease and severe degeneration of the central nervous system. Subject to post-translational internal peptidase cleavage, GNS is encoded by a gene mapping to human chromosome 12q14.2 and mouse chromosome 10 D2.


Catalog Number: (89269-098)
Supplier: Genetex
Description: Rabbit polyclonal antibody to HS3ST3B1 (N-terminal)


Catalog Number: (10298-886)
Supplier: Bioss
Description: GNS is a 552 amino acid lysosomal enzyme that hydrolyzes the 6-sulfate groups of the N-acetyl-D-glucosamine 6-sulfate units of keratan sulfate and heparan sulfate. A member of the sulfatase family, GNS assists in the catabolism of heparin, and binds calcium as a cofactor. GNS deficiency results in an autosomal recessive lysosomal storage disorder known as mucopolysaccharidosis type IIID (Sanfilippo D syndrome), which is characterized by mild somatic disease and severe degeneration of the central nervous system. Subject to post-translational internal peptidase cleavage, GNS is encoded by a gene mapping to human chromosome 12q14.2 and mouse chromosome 10 D2.


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