
Digoxigenin NHS-ester | CAS 129273-26-3
| Catalog Number | R01-0476 |
| Category | NHS Esters |
| Molecular Formula | C35H50N2O10 |
| Molecular Weight | 658.78 |
| Catalog Number | Size | Price | Quantity |
|---|---|---|---|
| R01-0476 | 5 mg | $1199 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
Digoxigenin NHS-ester is a digoxin cross-linking reagent.
Chemical Information
Product Specification
Application
Chemical Information
| Synonyms | (3β,5β,12β)-3-[2-[[6-[(2,5-Dioxo-1-pyrrolidinyl)oxy]-6-oxohexyl]amino]-2-oxoethoxy]-12,14-dihydroxycard-20(22)-enolide; DIG NHS; ε-(Digoxigenin-3-O-acetamido)caproic acid N-hydroxysuccinimide ester; Digoxigenin-3-O-methylcarbonyl-ε-aminocaproic acid-N-hydroxysuccinimide ester |
| Purity | 95% |
| IUPAC Name | (2,5-dioxopyrrolidin-1-yl) 6-[[2-[[(3S,5R,8R,9S,10S,12R,13S,17R)-12,14-dihydroxy-10,13-dimethyl-17-(5-oxo-2H-furan-3-yl)-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-yl]oxy]acetyl]amino]hexanoate |
| SMILES | CC12CCC(CC1CCC3C2CC(C4(C3(CCC4C5=CC(=O)OC5)O)C)O)OCC(=O)NCCCCCC(=O)ON6C(=O)CCC6=O |
| InChI | InChI=1S/C35H50N2O10/c1-33-13-11-23(45-20-28(39)36-15-5-3-4-6-31(42)47-37-29(40)9-10-30(37)41)17-22(33)7-8-25-26(33)18-27(38)34(2)24(12-14-35(25,34)44)21-16-32(43)46-19-21/h16,22-27,38,44H,3-15,17-20H2,1-2H3,(H,36,39)/t22-,23+,24-,25-,26+,27-,33+,34+,35?/m1/s1 |
| InChIKey | KHNDABJZSPPYLE-MZARVJLWSA-N |
| Solubility | soluble in Chloroform, DMSO |
| Density | 1.3±0.1 g/cm3 |
| Appearance | White to Light Brown Solid |
Product Specification
| Storage | Store at -20°C, Under inert atmosphere |
Application
Digoxigenin NHS-ester is a reactive digoxigenin derivative designed for efficient coupling to primary amines via NHS-ester chemistry, producing stable amide linkages under standard bioconjugation conditions. As a widely used bioorthogonal-compatible hapten, digoxigenin is commonly selected for high-specificity detection in immunoassays and nucleic-acid workflows, where the conjugated hapten serves as a molecular handle for anti-digoxigenin reagents. This reagent is therefore a practical choice for preparing labeled antibodies, oligonucleotide conjugates, and other amine-containing biomolecules or surfaces that require robust, assay-ready digoxigenin presentation.
1. Nucleic Acid Labeling
Digoxigenin NHS-ester is frequently used to introduce digoxigenin haptens onto amine-modified oligonucleotides, enabling sensitive probe and target labeling for hybridization-based assays. Research groups developing DNA and RNA detection workflows rely on digoxigenin to generate probes that can be visualized using anti-digoxigenin antibodies conjugated to enzymes, fluorophores, or chemiluminescent reporters. The NHS-ester format supports straightforward conjugation to amine-bearing linkers or modified nucleic acid backbones, which is particularly useful when building standardized probe sets for screening, mapping, and assay optimization.
2. Immunoassay Probe Conjugates
Digoxigenin NHS-ester is widely applied to prepare digoxigenin-tagged detection reagents for immunoassay formats, including antibody-based binding assays and antigen/ligand detection panels. By coupling digoxigenin to amine-containing proteins, peptides, or affinity reagents, laboratories create consistent hapten density for downstream recognition by anti-digoxigenin reagents. This approach is commonly used in research and industrial assay development to generate labeled standards, calibration materials, and assay components where a stable hapten tag improves workflow reproducibility and signal generation with established anti-digoxigenin detection systems.
3. Antibody and Protein Conjugation
Digoxigenin NHS-ester supports site-agnostic hapten installation on antibodies and other proteinaceous binders that present accessible primary amines, allowing construction of digoxigenin-functionalized biorecognition tools. Bioconjugation teams use this reagent to generate hapten-bearing proteins for use as assay reagents, binding controls, or as capture/detection elements in multi-step workflows that require orthogonal labeling strategies. The NHS-ester reactivity is particularly useful when preparing amine-rich conjugates such as carrier proteins, enzyme conjugates, or protein standards that must be compatible with anti-digoxigenin readouts.
4. Surface and Bead Functionalization
Digoxigenin NHS-ester is commonly used to functionalize amine-presenting solid supports, including activated beads, membranes, and polymeric surfaces, to create digoxigenin-displaying capture platforms. Diagnostic reagent developers and assay engineers use these materials to immobilize hapten tags for subsequent binding to anti-digoxigenin antibodies or conjugates, enabling modular assay assembly and streamlined washing-based workflows. This surface functionalization strategy is also used to build reference materials and binding controls where spatially localized hapten presentation can improve assay consistency across batches and formats.
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