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Katalogové číslo: (APOSOR28962-1G)

Dodavatel: Apollo Scientific

Popis: N-Acetyl-α-D-glucosamine

Měrná jednotka: 1 * 1 g

Akce

Dodavatel: Cayman Chemical

Popis: N-Acetyl-β-D-glucosamine

Dodavatel: Thermo Scientific

Popis: N-Acetyl-α-D-glucosamine 99+%

Bezpečnostní list

Dodavatel: Thermo Scientific

Popis: N-Acetyl-β-D-glucosamine 98%

Bezpečnostní list Certifikáty

Dodavatel: Apollo Scientific

Popis: From synthetic source.

Dodavatel: Apollo Scientific

Popis: N-Acetyl-β-D-glucosamine 95%

Katalogové číslo: (APOSOR3381-250MG)

Dodavatel: Apollo Scientific

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

Měrná jednotka: 1 * 250 mg

Akce

Dodavatel: Cayman Chemical

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

Dodavatel: Apollo Scientific

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

Dodavatel: Apollo Scientific

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

Dodavatel: Thermo Scientific

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

Bezpečnostní list Certifikáty

Katalogové číslo: (USBIG3040-89)

Dodavatel: US Biological

Popis: Anti-Glucosamine Rabbit Polyclonal Antibody

Měrná jednotka: 1 * 200 µl

Akce

Katalogové číslo: (BOSSBS-13479R-A680)

Dodavatel: Bioss

Popis: 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.

Měrná jednotka: 1 * 100 µl

Akce

Katalogové číslo: (BOSSBS-13479R-A750)

Dodavatel: Bioss

Popis: 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.

Měrná jednotka: 1 * 100 µl

Akce

Katalogové číslo: (BOSSBS-13479R-CY7)

Dodavatel: Bioss

Popis: 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.

Měrná jednotka: 1 * 100 µl

Akce

Katalogové číslo: (BOSSBS-13479R-A647)

Dodavatel: Bioss

Popis: 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.

Měrná jednotka: 1 * 100 µl

Akce