NEU2 Fluorogenic Assay Kit

Catalog #
82139
$650 *
Size: 96 reactions
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*US Pricing only. For international pricing, please contact your local distributor.
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Description

The NEU2 Fluorogenic Assay Kit is designed to measure NEU2 (Neuroaminidase 2 or Sialidase-2) glycohydrolase activity for screening and profiling applications. It comes in a convenient 96-well format, with purified recombinant NEU2 enzyme, NEU2 substrate, NEU2 assay buffer, and Stop Solution for 100 enzyme reactions. The NEU2 inhibitor NCGC00063279 is also included as a control.

Hydrolysation of the NEU substrate releases a fluorophore (λexc/λem = 365 nm/445 nm). The increase in fluorescence at λ=445 nm is directly proportional to NEU2 activity. 

Need us to run inhibitor screens or profile your compounds against NEU2? Check out our Metabolic Enzyme Screening Services

Synonyms
Cytosolic sialidase, N-acetyl-alpha-neuraminidase 2
Product Info
Storage and Usage
Citations
Assay Kit Format
Fluorogenic
Materials Required But Not Supplied
  • Fluorescent microtiter plate reader capable of measurement at λex355-375/λem435-455 nm.
  • Orbital shaker.
Format
Catalog # Name Amount Storage
101722 NEU2, His-Tag* 3 µg -80°C
  NEU2 Assay Buffer 5 ml -20°C
  25 mM NEU2 Substrate 10 µl -20°C
  5x Stop Solution 3 ml -20°C
  N-Acetyl-2,3-dehydro-2-deoxyneuraminic acid 300 μg -20°C
79685 96-well black microplate 1 Room Temp

* The concentration of protein is lot-specific and will be indicated on the tube containing the protein.

UniProt #
Q9Y3R4
Background

NEU2, also known as N-acetyl-alpha-neuroaminidase 2 or sialidase-2, belongs to the glycohydrolytic enzyme family. Glycoside hydrolases remove terminal sialic acid residues from sialo-glycoproteins and sialo-glycolipids. The human cytosolic sialidase NEU2 recognizes not only the a(2-3), a(2-8), and a(2-6) of the sialosyl linkage of the terminal sialic acid residue but also the inner sugar(s) of the oligosaccharide moiety, as well as the supramolecular organization of gangliosides. NEU2 has been implicated in several diseases such as cancer and type I and type II sialidosis. The PI3K-AKT pathway is upregulated in many cancers, with many of the proteins involved in this pathway being altered by sialylation, which can result in oncogene inactivation. Lower than average levels of NEU2 have been found in pancreatic cancer cells, resulting in decreased apoptosis. Inhibition of NEU2 is an important approach to decipher sialidase function and mechanism of action. The use of inhibitors may also prove useful as a therapeutic approach.

References

Khedri Z, et al., 2012, Org. Biomol. Chem 10: 6112-6120.
Mozzi A, et al., 2011, Proteins 80: 1123-1132.
Nath S., et al., 2018, Cell Death and Disease 9: 210.