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N-Acetyl-β-D-glucosamine

Supplier: Cayman Chemical
Description: N-Acetyl-β-D-glucosamine

Certificates

Image Unavailable-APOSOR28962-1G

N-Acetyl-α-D-glucosamine

Catalog Number: (APOSOR28962-1G)
Supplier: Apollo Scientific
Description: N-Acetyl-α-D-glucosamine
UOM: 1 * 1 g

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Image Unavailable-APOSBIA1710-5G

N-Acetyl-β-D-glucosamine

Supplier: Apollo Scientific
Description: From synthetic source.

Image Unavailable-APOSOR7800T-100G

N-Acetyl-β-D-glucosamine 95%

Supplier: Apollo Scientific
Description: N-Acetyl-β-D-glucosamine 95%

Image Unavailable-APOSOR3381-250MG

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

Catalog Number: (APOSOR3381-250MG)
Supplier: Apollo Scientific
Description: 1,3,4,6-Tetra-O-acetyl-β-D-glucosamine hydrochloride 98%
UOM: 1 * 250 mg
Image Unavailable-CAYM17867-5

2-Acetamido-1,3,4,6-tetra-O-acetyl-2-deoxy-β-D-glucopyranose ≥95%

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

Image Unavailable-APOSBICL4009-25G

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

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

Product Image-USBIG3040-89

Anti-Glucosamine Rabbit Polyclonal Antibody

Catalog Number: (USBIG3040-89)
Supplier: US Biological
Description: Anti-Glucosamine Rabbit Polyclonal Antibody
UOM: 1 * 200 µl
Image Unavailable-APOSBIA1238-5G

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

Supplier: Apollo Scientific
Description: 2-Acetamido-1,3,4,6-tetra-O-acetyl-2-deoxy-β-D-glucopyranose

Image Unavailable-L09020.03

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

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

SDS Certificates

Image Unavailable-BOSSBS-13479R-A680

Anti-Glucosamine 6 sulfatase Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Catalog Number: (BOSSBS-13479R-A680)
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.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13479R-A750

Anti-Glucosamine 6 sulfatase Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Catalog Number: (BOSSBS-13479R-A750)
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.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13479R-A488

Anti-GNS Rabbit Polyclonal Antibody (Alexa Fluor® 488)

Catalog Number: (BOSSBS-13479R-A488)
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.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13479R-CY7

Anti-GNS Rabbit Polyclonal Antibody (Cy7®)

Catalog Number: (BOSSBS-13479R-CY7)
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.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13479R-HRP

Anti-GNS Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Catalog Number: (BOSSBS-13479R-HRP)
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.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13479R-A647

Anti-GNS Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Catalog Number: (BOSSBS-13479R-A647)
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.
UOM: 1 * 100 µl
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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us on 0800 22 33 44.
Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us on 0800 22 33 44
Additional Documentation may be needed to purchase this item. A VWR representative will contact you if needed.
Additional Documentation may be needed to purchase this item. A VWR representative will contact you if needed.
This product has been blocked by your organisation. Please contact your purchasing department for more information.
The original product is no longer available. The replacement shown is available.
Product(s) marked with this symbol are discontinued - sold till end of stock. Alternatives may be available by searching with the VWR Catalogue Number listed above. If you need further assistance, please call VWR Customer Service on 0800 22 33 44.
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