Oligosaccharides

<p>6'-a-Sialyl-N-acetyllactosamine-sp-biotin is a recombinant modified oligosaccharide. It is an Oligosaccharide that is synthesized by the methylation of 6'-sialyllactose with acetic anhydride and triethylamine in DMF. It has a molecular weight of 805.00 Da and a CAS number of 1038746-08-5. 6'-a-Sialyl-N-acetyllactosamine-sp-biotin may be used as a monomer for click chemistry, as well as for other applications in carbohydrate chemistry, such as the synthesis of polysaccharides and complex carbohydrates. This product has high purity and can be custom synthesized to order.</p>

<p>Inhibitor of conversion of primary bile acids to secondary bile acids</p>

<p>Sodium alginate is a soluble fiber that is extracted from brown seaweed. It is a natural carbohydrate that can be modified to create a variety of sugar-based derivatives, such as Oligosaccharides, Monosaccharides, and Custom Synthesis. Sodium alginate has been modified with Fluorination, Methylation, Glycosylation, and Click Modification to create high-purity products for various applications.</p>

<p>2-Acetamido-6-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-2,3,4,6-tetraacetamido-2,3,4,6,-tetra deoxygalactose is an acetylated disaccharide that is used in the synthesis of 6 fluoro 3 indoxyl beta D galactopyranoside. It is a residue of polysaccharides and proteins. 2 Acetamido 6 O 2 acetamido 2 deoxy β D glucopyranosyl 2 deoxy D galactopyranose is a disaccharide that can be found as a component of many polysaccharides and proteins.</p>

<p>Lewis X trisaccharide-sp-biotin is a synthetic compound with fluorination, monosaccharide, and oligosaccharide. The sugar is a complex carbohydrate. It is synthesized by glycosylation and polysaccharide modification. The product has high purity and is custom synthesis for research purposes only. This product does not have CAS number because it is a custom synthesis.</p>

<p>Chondroitin disaccharide di-diSB trisodium salt is a chondroitin sulfate binding agent that can be used in the diagnosis of subcutaneous tumors. It binds to the chondroitin sulfate component of proteoglycans and stains these proteins under light microscopy. This agent can also be used to detect monoclonal antibodies that bind to the chondroitin sulfate component of proteoglycans. The detection of this agent may be done by enzyme-linked immunosorbent assay or fluorescence microscopy.</p>

<p>Blood group B antigen conjugated to spacer arm and biotin</p>

<p>Potential prebiotic oligosaccharides made from agar by enzymatic hydrolysis</p>

<p>2-Acetamido-2-deoxy-4-O-(b-D-galactopyranosyl)-D-glucopyranose LacNAc isomer. This compound has been shown to inhibit pro-inflammatory cytokines in human bronchial epithelial cell lines, which may be helpful in treating inflammatory conditions. The compound can be analyzed using high-performance liquid chromatography (HPLC), which separates molecules based on their chemical properties. The acid residues present in the molecule make it an ideal target for antibodies and polymer-based drug delivery systems. In host cells, this compound is involved in various biological processes related to cell adhesion and signaling.</p>

<p>Chondroitin disaccharide 6S sodium salt is a synthetic, fluorinated, oligosaccharide that has been custom synthesized and glycosylated. It is a sugar-based compound with a high purity and excellent solubility in water. It was synthesized by click modification of the sugar monomer with an amine group at the reducing end. The chondroitin disaccharide 6S sodium salt was further modified with methylation to yield a product with a higher purity.</p>

<p>Please enquire for more information about 1,5-α-L-Arabinooctaose including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1,5-α-L-Arabinohexaose is a carbohydrate. It is a nonreducing sugar that can be found in plants. 1,5-α-L-Arabinohexaose has an optimum pH of 5 and an ethanol concentration of 0.02%. The enzyme form of 1,5-α-L-Arabinohexaose is α-(1→6)-glycosidase. This enzyme hydrolyzes the α-(1→6) glycosidic bond between two glucose residues in a polysaccharide chain to produce β-(1→4) bonds. It also hydrolyzes the β-(1→4) glycosidic bond between two galactose residues to produce β-(1→2) bonds and oxidizes the terminal carbon atom to produce aldehyde products.<br>A structural analysis of this carbohydrate was conducted using marine microorganisms and it was found that they contain galacturonic acid and sugar residues</p>