-
Oligosaccharides
-
Free oligosaccharides
- Ganglioside oligosaccharides
- Alginate
- Fructan
- Galacturonan / Apiogalacturonan
- Glucan
- Core Structures
- Blood group antigens
- Lewis antigens
- Fucosylated oligosaccharides
- Galα-3Gal oligosaccharides
- Sialylated oligosaccharides
- Globoside oligosaccharides
- Di-. Tri-. Tetrasaccharides
- Miscellaneous
- Oligosaccharide analogues
- Glucuronylated oligosaccharides
- Mannan
- Ulvan
- Xylan
- Labelled oligosaccharides
- Protected oligosaccharides
-
Spacer-armed oligosaccharides
- Monosaccharides
-
Free oligosaccharides
-
Glycoconjugates
- Spacer-armed oligosaccharides
-
Biotinylated oligosaccharides
- Biotinylated Ganglioside oligosaccharides
- Biotinylated Blood group antigens
- Biotinylated Lewis antigens
- Biotinylated Globoside oligosaccharides
- Biotinylated Cello-oligosaccharides
- Biotinylated Core structures
- Biotinylated Galili antigens
- Biotinylated Human milk oligosaccharides
- Biotinylated Isoglobo oligosaccharides
- Biotinylated Malto-oligosaccharides
- Affinity absorbant
- Neoglycoprotein - BSA
-
Neoglycoproteins - BSA
- Neoglycoproteins - KLH
- Polysaccharides
- Lectins
- Analytical References
- Analysis
- Research services
- Company
Fucosyl GM1 Ganglioside oligosaccharide-NAc-propargyl (Sodium salt)
Product code: GLY103-NPR
Fucα1-2Galβ1-3GalNAcβ1-4(Neu5Acα2-3)Galβ1-4Glc-NAc-CH2-CΞCH
Clickable Fucosyl GM1 oligosaccharide. The hexaccharide is conjugated with a spacer-arm ending by a propragy function for grafting by the copper-catalized azide-alkyne cycloaddition (CuAAC / Azide-alkyne Huisgen cycloaddition)
Packaging
Price
Quantity
Chemical formula: C48 H76 N3 O33 Na1
Molecular weight: 1246.11
Laboratory reagent for research and development only. Not for human or animal use.
specs_GLY103_NPR.pdf (specs_GLY103_NPR.pdf)
Download
(122.32k)
MSDS_GLY103_NPR.pdf (MSDS_GLY103_NPR.pdf)
Download
(288.89k)
You might also like
Clickable Fucosyl GM1 oligosaccharide. The hexaccharide is conjugated with a spacer-arm ending by a propragy function for grafting by the copper-catalized azide-alkyne cycloaddition (CuAAC / Azide-alkyne Huisgen cycloaddition)