Sialoside Array

10606

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The Sialoside Array allows researchers to explore the interactions between sialosides and various biological samples, for example, proteins, antibodies, cells, cell lysate, serum, vesicles, bacteria, or viral particles. The array features 50 structurally defined N-glycans and LacNAc glycans, each paired with Neu5Gc and Neu5Ac at the non-reducing end. Each array contains 8 or 16 identical subarrays, enabling the simultaneous analysis of multiple samples. The Sialoside Array provides high-throughput and reliable sialoside-binding information with a simple assay format that only requires a small sample volume. Results can be obtained in only a few hours, making investigating sialoside binding easy and efficient. To accommodate specific research needs, the Sialoside Array can be customized, and assay services are available upon request.

Explore how the Sialoside Array advances influenza research by revealing receptor specificity, host adaptation, and viral evolution.

SKU: 10606 Category:
Description
Structures
Examples
Citations
Document

Description

Sialosides are sialic acid-containing carbohydrates that are widely present on the surface of mammalian cells. The diversity of sialosides stems from variations in sialic acid linkages, sialic acid modifications such as acetylation, and underlying glycan structures. Among these, N-acetylneuraminic acid (Neu5Ac) and N-glycolylneuraminic acid (Neu5Gc) are two predominant forms of sialic acid that influence a range of biological functions.

Sialosides play essential roles in many biological processes by acting as key recognition molecules. They are involved in cell-cell communication, immune modulation, pathogen-host interactions, and cancer progression. In the immune system, sialosides interact with lectins such as Siglecs and selectins, regulating immune cell activation and inflammation. Many viruses, including influenza, and bacteria, such as Helicobacter pylori, recognize sialosides as entry receptors to establish infections. Additionally, aberrant sialylation is frequently observed in cancer, where tumor cells exploit altered sialoside expression to evade immune surveillance and enhance metastasis. Despite their biological importance, the study of sialoside interactions has been challenging due to limited access to well-defined sialylated structures.

The Sialoside Array provides a powerful tool to investigate sialoside-mediated interactions with biological samples, including proteins, antibodies, cells, cell lysates, serum, vesicles, bacteria, and viral particles. The array consists of 50 structurally defined N-glycans and LacNAc glycans, each systematically paired with Neu5Gc and Neu5Ac at the non-reducing end. This design allows researchers to compare binding preferences and functional differences between these two forms of sialic acid.

Each array contains 8 or 16 identical subarrays, enabling simultaneous analysis of multiple samples for high-throughput experimentation. The platform offers a simple assay format requiring only a small sample volume, providing reliable and reproducible glycan-binding data within a few hours.

Features

  • 50 Sialoside structures;
  • Unrivaled sensitivity and specificity;
  • Simple assay format;
  • Small sample volume;
  • Customizable (select glycans for a specific microarray format)
  • Assay service available;

Applications

  • Evaluate binding specificities of sialoside-interacting proteins;
  • Evaluate binding specificities of sialoside-interacting antibodies;
  • Study virus – sialoside interactions;
  • Study bacteria – sialoside interactions;
  • Study vesicle – sialoside interactions;
  • Study cell – sialoside interactions;

Structures

List of Sialoside structures on the array (download the PDF)

Glycan ID Glycan Name
SA1 Neu5Acα2-3Galβ1-4GlcNAcβ1-2Manα1-6(Neu5Acα2-3Galβ1-4GlcNAcβ1-2Manα1-3)Manβ1-4GlcNAcβ1-4GlcNAc-
SA2 Neu5Gcα2-3Galβ1-4GlcNAcβ1-2Manα1-6(Neu5Gcα2-3Galβ1-4GlcNAcβ1-2Manα1-3)Manβ1-4GlcNAcβ1-4GlcNAc-
SA3 Neu5Acα2-6Galβ1-4GlcNAcβ1-2Manα1-6(Neu5Acα2-6Galβ1-4GlcNAcβ1-2Manα1-3)Manβ1-4GlcNAcβ1-4GlcNAc-
SA4 Neu5Gcα2-6Galβ1-4GlcNAcβ1-2Manα1-6(Neu5Gcα2-6Galβ1-4GlcNAcβ1-2Manα1-3)Manβ1-4GlcNAcβ1-4GlcNAc-
SA5 Manα1-6(Manα1-3)Manα1-6(Neu5Acα2-3Galβ1-4GlcNAcβ1-2Manα1-3)Manβ1-4GlcNAcβ1-4GlcNAc-
SA6 Manα1-6(Manα1-3)Manα1-6(Neu5Gcα2-3Galβ1-4GlcNAcβ1-2Manα1-3)Manβ1-4GlcNAcβ1-4GlcNAc-
SA7 Manα1-6(Manα1-3)Manα1-6(Neu5Acα2-6Galβ1-4GlcNAcβ1-2Manα1-3)Manβ1-4GlcNAcβ1-4GlcNAc-
SA8 Manα1-6(Manα1-3)Manα1-6(Neu5Gcα2-6Galβ1-4GlcNAcβ1-2Manα1-3)Manβ1-4GlcNAcβ1-4GlcNAc-
SA9 Manα1-6(Manα1-3)Manα1-6(Neu5Acα2-3Galβ1-4(Fucα1-3)GlcNAcβ1-2Manα1-3)Manβ1-4GlcNAcβ1-4GlcNAc-
SA10 Manα1-6(Manα1-3)Manα1-6(Neu5Gcα2-3Galβ1-4(Fucα1-3)GlcNAcβ1-2Manα1-3)Manβ1-4GlcNAcβ1-4GlcNAc-
SA11 Neu5Acα2-3Galβ1-4GlcNAcβ1-2Manα1-3Manβ1-4GlcNAcβ1-4GlcNAc-
SA12 Neu5Gcα2-3Galβ1-4GlcNAcβ1-2Manα1-3Manβ1-4GlcNAcβ1-4GlcNAc-
SA13 Neu5Acα2-6Galβ1-4GlcNAcβ1-2Manα1-3Manβ1-4GlcNAcβ1-4GlcNAc-
SA14 Neu5Gcα2-6Galβ1-4GlcNAcβ1-2Manα1-3Manβ1-4GlcNAcβ1-4GlcNAc-
SA15 Neu5Acα2-3Galβ1-4(Fucα1-3)GlcNAcβ1-2Manα1-3Manβ1-4GlcNAcβ1-4GlcNAc-
SA16 Neu5Gcα2-3Galβ1-4(Fucα1-3)GlcNAcβ1-2Manα1-3Manβ1-4GlcNAcβ1-4GlcNAc-
SA17 Neu5Acα2-3Galβ1-4GlcNAcβ1-2Manα1-6Manβ1-4GlcNAcβ1-4GlcNAc-
SA18 Neu5Gcα2-3Galβ1-4GlcNAcβ1-2Manα1-6Manβ1-4GlcNAcβ1-4GlcNAc-
SA19 Neu5Acα2-6Galβ1-4GlcNAcβ1-2Manα1-6Manβ1-4GlcNAcβ1-4GlcNAc-
SA20 Neu5Gcα2-6Galβ1-4GlcNAcβ1-2Manα1-6Manβ1-4GlcNAcβ1-4GlcNAc-
SA21 Neu5Acα2-3Galβ1-4(Fucα1-3)GlcNAcβ1-2Manα1-6Manβ1-4GlcNAcβ1-4GlcNAc-
SA22 Neu5Gcα2-3Galβ1-4(Fucα1-3)GlcNAcβ1-2Manα1-6Manβ1-4GlcNAcβ1-4GlcNAc-
SA23 Neu5Acα2-3Galβ1-4GlcNAcβ1-2Manα1-6(Manα1-3)Manβ1-4GlcNAcβ1-4GlcNAc-
SA24 Neu5Gcα2-3Galβ1-4GlcNAcβ1-2Manα1-6(Manα1-3)Manβ1-4GlcNAcβ1-4GlcNAc-
SA25 Neu5Acα2-3Galβ1-4(Fucα1-3)GlcNAcβ1-2Manα1-6(Manα1-3)Manβ1-4GlcNAcβ1-4GlcNAc-
SA26 Neu5Gcα2-3Galβ1-4(Fucα1-3)GlcNAcβ1-2Manα1-6(Manα1-3)Manβ1-4GlcNAcβ1-4GlcNAc-
SA27 GlcNAcβ1-2Manα1-6(Neu5Acα2-3Galβ1-4GlcNAcβ1-2Manα1-3)Manβ1-4GlcNAcβ1-4GlcNAc-
SA28 GlcNAcβ1-2Manα1-6(Neu5Gcα2-3Galβ1-4GlcNAcβ1-2Manα1-3)Manβ1-4GlcNAcβ1-4GlcNAc-
SA29 GlcNAcβ1-2Manα1-6(Neu5Acα2-3Galβ1-4(Fucα1-3)GlcNAcβ1-2Manα1-3)Manβ1-4GlcNAcβ1-4GlcNAc-
SA30 GlcNAcβ1-2Manα1-6(Neu5Gcα2-3Galβ1-4(Fucα1-3)GlcNAcβ1-2Manα1-3)Manβ1-4GlcNAcβ1-4GlcNAc-
SA31 Neu5Acα2-3Galβ1-4GlcNAcβ1-2Manα1-6(Galβ1-4(Fucα1-3)GlcNAcβ1-2Manα1-3)Manβ1-4GlcNAcβ1-4GlcNAc-
SA32 Neu5Gcα2-3Galβ1-4GlcNAcβ1-2Manα1-6(Galβ1-4(Fucα1-3)GlcNAcβ1-2Manα1-3)Manβ1-4GlcNAcβ1-4GlcNAc-
SA33 Neu5Acα2-6Galβ1-4GlcNAcβ1-2Manα1-6(Galβ1-4(Fucα1-3)GlcNAcβ1-2Manα1-3)Manβ1-4GlcNAcβ1-4GlcNAc-
SA34 Neu5Gcα2-6Galβ1-4GlcNAcβ1-2Manα1-6(Galβ1-4(Fucα1-3)GlcNAcβ1-2Manα1-3)Manβ1-4GlcNAcβ1-4GlcNAc-
SA35 Neu5Acα2-6Galβ1-4GlcNAcβ1-2Manα1-6(Neu5Acα2-3Galβ1-4(Fucα1-3)GlcNAcβ1-2Manα1-3)Manβ1-4GlcNAcβ1-4GlcNAc-
SA36 Neu5Gcα2-6Galβ1-4GlcNAcβ1-2Manα1-6(Neu5Gcα2-3Galβ1-4(Fucα1-3)GlcNAcβ1-2Manα1-3)Manβ1-4GlcNAcβ1-4GlcNAc-
SA37 Neu5Acα2-3Galβ1-4GlcNAcβ1-2Manα1-6(GlcNAcβ1-2Manα1-3)Manβ1-4GlcNAcβ1-4GlcNAc-
SA38 Neu5Gcα2-3Galβ1-4GlcNAcβ1-2Manα1-6(GlcNAcβ1-2Manα1-3)Manβ1-4GlcNAcβ1-4GlcNAc-
SA39 Neu5Acα2-6Galβ1-4GlcNAcβ1-2Manα1-6(GlcNAcβ1-2Manα1-3)Manβ1-4GlcNAcβ1-4GlcNAc-
SA40 Neu5Gcα2-6Galβ1-4GlcNAcβ1-2Manα1-6(GlcNAcβ1-2Manα1-3)Manβ1-4GlcNAcβ1-4GlcNAc-
SA41 Neu5Acα2-3Galβ1-4GlcNAcβ1-2Manα1-6(Galβ1-4GlcNAcβ1-2Manα1-3)Manβ1-4GlcNAcβ1-4GlcNAc-
SA42 Neu5Gcα2-3Galβ1-4GlcNAcβ1-2Manα1-6(Galβ1-4GlcNAcβ1-2Manα1-3)Manβ1-4GlcNAcβ1-4GlcNAc-
SA43 Neu5Acα2-6Galβ1-4GlcNAcβ1-2Manα1-6(Galβ1-4GlcNAcβ1-2Manα1-3)Manβ1-4GlcNAcβ1-4GlcNAc-
SA44 Neu5Gcα2-6Galβ1-4GlcNAcβ1-2Manα1-6(Galβ1-4GlcNAcβ1-2Manα1-3)Manβ1-4GlcNAcβ1-4GlcNAc-
SA45 Neu5Acα2-3Galβ1-4GlcNAcβ1-3Galβ1-4GlcNAcβ1-2Manα1-6(Neu5Acα2-3Galβ1-4GlcNAcβ1-3Galβ1-4GlcNAcβ1-2Manα1-3)Manβ1-4GlcNAcβ1-4GlcNAc-
SA46 Neu5Acα2-6Galβ1-4GlcNAcβ1-3Galβ1-4GlcNAcβ1-2Manα1-6(Neu5Acα2-6Galβ1-4GlcNAcβ1-3Galβ1-4GlcNAcβ1-2Manα1-3)Manβ1-4GlcNAcβ1-4GlcNAc-
SA47 Neu5Acα2-3Galβ1-4GlcNAcβ1-3Galβ1-4GlcNAcβ1-3Galβ1-4GlcNAcβ1-2Manα1-6(Neu5Acα2-3Galβ1-4GlcNAcβ1-3Galβ1-4GlcNAcβ1-3Galβ1-4GlcNAcβ1-2Manα1-3)Manβ1-4GlcNAcβ1-4GlcNAc-
SA48 Neu5Acα2-6Galβ1-4GlcNAcβ1-3Galβ1-4GlcNAcβ1-3Galβ1-4GlcNAcβ1-2Manα1-6(Neu5Acα2-6Galβ1-4GlcNAcβ1-3Galβ1-4GlcNAcβ1-3Galβ1-4GlcNAcβ1-2Manα1-3)Manβ1-4GlcNAcβ1-4GlcNAc-
SA49 Neu5Acα2-3Galβ1-4GlcNAcβ1-3Galβ1-4GlcNAcβ1-3Galβ1-4GlcNAcβ1-3Galβ1-4GlcNAcβ1-2Manα1-6(Neu5Acα2-3Galβ1-4GlcNAcβ1-3Galβ1-4GlcNAcβ1-3Galβ1-4GlcNAcβ1-3Galβ1-4GlcNAcβ1-2Manα1-3)Manβ1-4GlcNAcβ1-4GlcNAc-
SA50 Neu5Acα2-6Galβ1-4GlcNAcβ1-3Galβ1-4GlcNAcβ1-3Galβ1-4GlcNAcβ1-3Galβ1-4GlcNAcβ1-2Manα1-6(Neu5Acα2-6Galβ1-4GlcNAcβ1-3Galβ1-4GlcNAcβ1-3Galβ1-4GlcNAcβ1-3Galβ1-4GlcNAcβ1-2Manα1-3)Manβ1-4GlcNAcβ1-4GlcNAc-

Examples

Sambucus Nigra Lectin (SNA) binds to α-2,6 sialic acids

The Sialoside Array was assayed with biotinylated Sambucus Nigra Lectin (SNA) lectin (5 μg/mL), followed by streptavidin (Cy3). The array was scanned with a microarray scanner at 532nm wavelength. Positive control and marker showed bindings as expected. SNA preferentially binds to α-2,6 sialic acid-containing glycans.

Document

List of Sialoside structures on the array (download the PDF)

Protocol & User Manual (download the manual)