You Searched For: 6-Azido-6-deoxy-L-galactose


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Catalog Number: (CAYM18679-1)
Supplier: Cayman Chemical
Description: 3'-Azido-3'-deoxythymidine -D-glucuronide (sodium salt) 1 * 1 mg
UOM: 1 * 1 mg


Catalog Number: (APOSBIBP1074-250MG)
Supplier: Apollo Scientific
Description: Azido triglycine-250mg pack 1 * 250 mg
UOM: 1 * 250 mg


Catalog Number: (APOSBICL4154-1MG)
Supplier: Apollo Scientific
Description: METHYL O-(6-O-ACETYL-2-AZIDO-3,4-DI-O-BE 1 * 1 mg
UOM: 1 * 1 mg


Catalog Number: (PRSI30-412)
Supplier: ProSci Inc.
Description: Galactose-1-phosphate uridyl transferase (GALT) catalyzes the second step of the Leloir pathway of galactose metabolism, namely the conversion of UDP-glucose + galactose-1-phosphate to glucose-1-phosphate + UDP-galactose. The absence of this enzyme results in classic galactosemia in humans and can be fatal in the newborn period if lactose is not removed from the diet. The pathophysiology of galactosemia has not been clearly defined. Galactose-1-phosphate uridyl transferase (GALT) catalyzes the second step of the Leloir pathway of galactose metabolism, namely the conversion of UDP-glucose + galactose-1-phosphate to glucose-1-phosphate + UDP-galactose. The absence of this enzyme results in classic galactosemia in humans and can be fatal in the newborn period if lactose is not removed from the diet. The pathophysiology of galactosemia has not been clearly defined. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
UOM: 1 * 50 µG


Catalog Number: (APOSOR88099-100MG)
Supplier: Apollo Scientific
Description: 1-Azido-4-bromobutane 100mg pack 1 * 100 mg
UOM: 1 * 100 mg

New Product


Catalog Number: (APOSBICL2506-1G)
Supplier: Apollo Scientific
Description: PHENYL 3,4,6-TRI-O-ACETYL-2-AZIDO-2-DEOX 1 * 1 g
UOM: 1 * 1 g


Catalog Number: (APOSOR36386-250MG)
Supplier: Apollo Scientific
Description: BOC-P-AZIDO-PHE-OH 1 * 250 mg
UOM: 1 * 250 mg


Catalog Number: (BOSSBS-13267R-HRP)
Supplier: Bioss
Description: GALK2 is important in the first step of the galactose metabolism pathway. GALK1, which belongs to the GHMP kinase family of proteins, is a crucial enzyme for galactose metabolism, specifically converting ?d-galactose to galactose 1-phosphate. Defects in the gene encoding GALK1 can cause galactosemia II, an autosomal recessive disorder characterized by congenital cataracts during infancy, often within the first two weeks of life. In the adult population, galactosemia II can cause presenile cataracts that are secondary to accumulation of galactitol in the lens of the eye. A second gene, GALK2, encodes an enzyme with greater activity against GalNAc than galactose. GALK2 has been implicated in the salvage pathway for the reutilization of free GalNAc derived from the degradation of complex carbohydrates.
UOM: 1 * 100 µl


Catalog Number: (BOSSBS-13267R-CY3)
Supplier: Bioss
Description: GALK2 is important in the first step of the galactose metabolism pathway. GALK1, which belongs to the GHMP kinase family of proteins, is a crucial enzyme for galactose metabolism, specifically converting ?d-galactose to galactose 1-phosphate. Defects in the gene encoding GALK1 can cause galactosemia II, an autosomal recessive disorder characterized by congenital cataracts during infancy, often within the first two weeks of life. In the adult population, galactosemia II can cause presenile cataracts that are secondary to accumulation of galactitol in the lens of the eye. A second gene, GALK2, encodes an enzyme with greater activity against GalNAc than galactose. GALK2 has been implicated in the salvage pathway for the reutilization of free GalNAc derived from the degradation of complex carbohydrates.
UOM: 1 * 100 µl


Catalog Number: (BOSSBS-13267R-CY7)
Supplier: Bioss
Description: GALK2 is important in the first step of the galactose metabolism pathway. GALK1, which belongs to the GHMP kinase family of proteins, is a crucial enzyme for galactose metabolism, specifically converting ?d-galactose to galactose 1-phosphate. Defects in the gene encoding GALK1 can cause galactosemia II, an autosomal recessive disorder characterized by congenital cataracts during infancy, often within the first two weeks of life. In the adult population, galactosemia II can cause presenile cataracts that are secondary to accumulation of galactitol in the lens of the eye. A second gene, GALK2, encodes an enzyme with greater activity against GalNAc than galactose. GALK2 has been implicated in the salvage pathway for the reutilization of free GalNAc derived from the degradation of complex carbohydrates.
UOM: 1 * 100 µl


Catalog Number: (APOSPC250102-1G)
Supplier: Apollo Scientific
Description: 1-AZIDO-1H,1H,2H,2H-PERFLUOROOCTANE 1 * 1 g
UOM: 1 * 1 g


Catalog Number: (APOSOR79185-1G)
Supplier: Apollo Scientific
Description: (S)-2-Azido-3,3-dimethylbutanoic acid 1g pack 1 * 1 g
UOM: 1 * 1 g

New Product


Catalog Number: (CAYM18895-100)
Supplier: Cayman Chemical
Description: 1,6-Anhydro-D-galactose 1 * 100 mg
UOM: 1 * 100 mg


Catalog Number: (CAYM18895-500)
Supplier: Cayman Chemical
Description: 1,6-Anhydro-D-galactose 1 * 500 mg
UOM: 1 * 500 mg


Catalog Number: (APOSOR79185-5G)
Supplier: Apollo Scientific
Description: (S)-2-Azido-3,3-dimethylbutanoic acid 5g pack 1 * 5 g
UOM: 1 * 5 g

New Product


Catalog Number: (APOSOR88099-250MG)
Supplier: Apollo Scientific
Description: 1-Azido-4-bromobutane 250mg pack 1 * 250 mg
UOM: 1 * 250 mg

New Product


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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 +353 1 88 22222.
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 +353 1 88 22222.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at eurega_services@eu.vwr.com
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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 Catalog Number listed above. If you need further assistance, please call VWR Customer Service on +353 1 8822222.
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