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Sulfatide (bovine) (sodium salt)

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    Sulfatide (bovine) (sodium salt)
  • Sulfatide (bovine) (sodium salt)
Cat No: 24323
Biochemicals - Lipids
Cayman

Sulfatides are endogenous sulfoglycolipids with various biological activities in the central and peripheral nervous systems, pancreas, and immune system.{40646} They are produced from the combination of ceramide and UDP-galactose in the endoplasmic re...

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Territorial Availability: Available through Bertin Technologies only in France
Synonyms:
  • 1-O-(3-O-sulfo-?-D-galactopyranosyl)-ceramide, monosodium salt
Correlated keywords:
  • 85496-63-5 sulfolipid myelin cereboside SM4s gal-cer
Product Overview:
Sulfatides are endogenous sulfoglycolipids with various biological activities in the central and peripheral nervous systems, pancreas, and immune system.{40646} They are produced from the combination of ceramide and UDP-galactose in the endoplasmic reticulum followed by sulfation in the Golgi apparatus. The ceramide portion contains variable fatty acid chain lengths, which are tissue- and pathology-dependent. Sulfatides are primarily found in the myelin sheath of oligodendrocytes and Schwann cells, with smaller chain lengths predominant during development and longer chain lengths predominant in mature cells.{40648} They accumulate in the lysosome of patients with metachromatic leukodystrophy, a disorder characterized by arylsulfatase A deficiency.{40650,40646} Sulfatides are also located in pancreatic β-cells and inhibit insulin release from isolated rat pancreatic islet cells, suggesting a potential role in diabetes.{40644} Sulfatides can induce inflammation in glia in vitro and certain sulfatides, such as C24:1 3’-sulfo-galactosylceramide, can induce an immune response in vitro in mouse splenocytes.{40645,40651} Sulfatides (bovine) (sodium salt) is a mixture of isolated bovine sulfatides. [Matreya, LLC. Catalog No. 1049]
Size 1 mg
Shipping dry ice
Molecular Formula C42H80NO11S • Na (for stearoyl)
SMILES O[C@@H]1[C@@H](OS([O-])(=O)=O)[C@@H](O)[C@@H](CO)O[C@H]1OC[C@H](NC([R])=O)[C@H](O)/C=C/CCCCCCCCCCCCC.[Na+]
Molecular Weight 830,1
Formulation A solid
Purity ≥95%
Custom Code 2930.90
UNSPSC code 12352100

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Cayman Chemical's mission is to help make research possible by supplying scientists worldwide with the basic research tools necessary for advancing human and animal health. Our utmost commitment to healthcare researchers is to offer the highest quality products with an affordable pricing policy.

Our scientists are experts in the synthesis, purification, and characterization of biochemicals ranging from small drug-like heterocycles to complex biolipids, fatty acids, and many others. We are also highly skilled in all aspects of assay and antibody development, protein expression, crystallization, and structure determination.

Over the past thirty years, Cayman developed a deep knowledge base in lipid biochemistry, including research involving the arachidonic acid cascade, inositol phosphates, and cannabinoids. This knowledge enabled the production of reagents of exceptional quality for cancer, oxidative injury, epigenetics, neuroscience, inflammation, metabolism, and many additional lines of research.

Our organic and analytical chemists specialize in the rapid development of manufacturing processes and analytical methods to carry out clinical and commercial GMP-API production. Pre-clinical drug discovery efforts are currently underway in the areas of bone restoration and repair, muscular dystrophy, oncology, and inflammation. A separate group of Ph.D.-level scientists are dedicated to offering Hit-to-Lead Discovery and Profiling Services for epigenetic targets. Our knowledgeable chemists can be contracted to perform complete sample analysis for analytes measured by the majority of our assays. We also offer a wide range of analytical services using LC-MS/MS, HPLC, GC, and many other techniques.

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ISO/IEC 17025:2005
ISO Guide 34:2009

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