Votre recherche pour: N-Acétyl-\u03B2-D-glucosamine

Référence Produit: (APOSOR28962-1G)

Fournisseur: Apollo Scientific

Description: N-Acétyl-α-D-glucosamine

UOM: 1 * 1 g

*Promo

Fournisseur: Thermo Fisher Scientific

Description: N-Acétyl-β-D-glucosamine 98%

FDS (Fiche de données de sécurité)

Fournisseur: Thermo Fisher Scientific

Description: N-Acétyl-α-D-glucosamine 99+%

FDS (Fiche de données de sécurité)

Fournisseur: Cayman Chemical

Description: N-Acétyl-β-D-glucosamine

Certificats.

Fournisseur: Apollo Scientific

Description: From synthetic source.

Fournisseur: Apollo Scientific

Description: N-Acétyl-β-D-glucosamine 95%

Référence Produit: (APOSOR3381-250MG)

Fournisseur: Apollo Scientific

Description: 1,3,4,6-Tetra-O-acetyl-β-D-glucosamine hydrochloride 98%

UOM: 1 * 250 mg

*Promo

Fournisseur: Cayman Chemical

Description: β-D-Glucosamine pentaacetate is an N-acetylglucosamine derivative that has been shown to promote hyaluronic acid production.

Fournisseur: Apollo Scientific

Description: 2-Acetamido-1,3,4,6-tetra-O-acetyl-2-deoxy-D-glucopyranose ≥99%

Fournisseur: Thermo Fisher Scientific

Description: 2-Acetamido-1,3,4,6-tetra-O-acetyl-2-deoxy-β-D-glucopyranose 96%

FDS (Fiche de données de sécurité) Certificats.

Référence Produit: (BOSSBS-13479R-A680)

Fournisseur: 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.

UOM: 1 * 100 µl

*Promo

Référence Produit: (BOSSBS-13479R-A750)

Fournisseur: 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.

UOM: 1 * 100 µl

*Promo

Référence Produit: (BOSSBS-13479R-CY3)

Fournisseur: 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.

UOM: 1 * 100 µl

*Promo

Référence Produit: (BOSSBS-13479R-CY7)

Fournisseur: 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.

UOM: 1 * 100 µl

*Promo

Référence Produit: (BOSSBS-13479R-HRP)

Fournisseur: 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.

UOM: 1 * 100 µl

*Promo

Référence Produit: (BOSSBS-13479R-A647)

Fournisseur: 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.

UOM: 1 * 100 µl

*Promo