Europium-labeled monoclonal antibody recognizing O-linked n-acetylglucosamine (O-linked GlcNAc). For use in LANCE® Ultra post-translational modification assays.
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The LANCE® Ultra Europium-anti-anti-O-linked-GlcNAc antibody was used for the development and optimization of a O-GlcNAc hydrolase (OGA) assay using a biotinylated Tau-derived peptide O-GlcNAcylated at Ser400 as substrate. A technical note describing
the assay is available in our product literature.
Formats:
Proven, cost-efficient LANCE Ultra reagents can be used to quantitate peptide modifications, detecting specific meythylation and acetylation states. No wash, homogenous LANCE Ultra reagents are HTS friendly - design your own epigenetics screening strategy for greatest efficiency.
Epigenetic enzymatic assays are optimized using a biotinylated histone H3-derived peptide as substrate. The modified peptide is captured by the Eu-labeled antibody (Ab) and ULight-Streptavidin (SA) which bring the Eu donor and ULight acceptor dye molecules into close proximity. Upon irradiation at 320 or 340 nm, the energy from the Eu donor is transferred to the ULight acceptor dye which, in turn, generates light at 665 nm. The intensity of the light emission is proportional to the level of biotinylated substrate modification.
| Antibody Conjugates | Anti-O-linked-GlcNAc |
|---|---|
| Automation Compatible | Yes |
| Detection Method | Time-Resolved Fluorescence (TRF), TR-FRET |
| Experimental Type | In vitro |
| Fluorophore | Eu-W1024 |
| Molecular Modification | GlcNAc |
| Product Brand Name | LANCE Ultra |
| Shipping Condition | Dry Ice |
| Unit Size | 10 µg |
This LANCE Ultra immunodetection assay measures the hydrolysis of an O-GlcNAc moiety,from a biotinylated Tau-Ser400-O-GlcNAc peptide.
