Sie suchten nach: u0302

Lieferant: Cayman Chemical

Beschreibung: N-Acetyl-β-D-glucosamin

Zertifikate

Artikel-Nr: (APOSOR28962-1G)

Lieferant: Apollo Scientific

Beschreibung: N-Acetyl-α-D-glucosamin

VE: 1 * 1 g

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Lieferant: Thermo Scientific

Beschreibung: N-Acetyl-α-D-glucosamin 99+%

Sicherheitsdatenblätter

Lieferant: Thermo Scientific

Beschreibung: N-Acetyl-β-D-glucosamin 98%

Sicherheitsdatenblätter Zertifikate

Lieferant: Apollo Scientific

Beschreibung: From synthetic source.

Lieferant: Apollo Scientific

Beschreibung: N-Acetyl-β-D-glucosamin 95%

Artikel-Nr: (APOSOR3381-250MG)

Lieferant: Apollo Scientific

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

VE: 1 * 250 mg

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Lieferant: Cayman Chemical

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

Lieferant: Apollo Scientific

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

Lieferant: Apollo Scientific

Beschreibung: 2-Acetamido-1,3,4,6-tetra-O-acetyl-2-desoxy-β-D-glucopyranose

Lieferant: Thermo Scientific

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

Sicherheitsdatenblätter Zertifikate

Artikel-Nr: (USBIG3040-89)

Lieferant: US Biological

Beschreibung: Anti-Glucosamine Rabbit Polyclonal Antibody

VE: 1 * 200 µl

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Artikel-Nr: (BOSSBS-13479R-A680)

Lieferant: Bioss

Beschreibung: 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.

VE: 1 * 100 µl

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Artikel-Nr: (BOSSBS-13479R-A750)

Lieferant: Bioss

Beschreibung: 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.

VE: 1 * 100 µl

Sale!

Artikel-Nr: (BOSSBS-13479R-CY7)

Lieferant: Bioss

Beschreibung: 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.

VE: 1 * 100 µl

Sale!

Artikel-Nr: (BOSSBS-13479R-HRP)

Lieferant: Bioss

Beschreibung: 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.

VE: 1 * 100 µl

Sale!