
ATTO 610 maleimide
| Catalog Number | F10-0131 |
| Category | ATTO Dyes |
| Molecular Formula | C31H37ClN4O7 |
| Molecular Weight | 613.10 |
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Product Introduction
ATTO 610 maleimide is a thiol-reactive fluorophore that belongs to the class of xanthene dyes, known for its intense red fluorescence. It features a maleimide functional group, enabling efficient conjugation to sulfhydryl groups on proteins and peptides, making it suitable for protein labeling and molecular tracking applications. The dye exhibits strong absorption and emission characteristics, which are exploited in fluorescence microscopy and flow cytometry for precise imaging and analysis of biological samples.
Chemical Information
Product Specification
Application
Computed Properties
Chemical Information
| Synonyms | ATTO 610-4; atto610-maleimide; Atto 610 maleimide, BioReagent, suitable for fluorescence, >=90% (coupling to thiols); 4-[9-(dimethylamino)-11,11-dimethyl-3,4-dihydro-2H-naphtho[2,3-g]quinolin-1-ium-1-yl]-N-[2-(2,5-dioxopyrrol-1-yl)ethyl]butanamide;perchlorate; 9-(dimethylamino)-1-(4-{[2-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)ethyl]amino}-4-oxobutyl)-11,11-dimethyl-2,3,4,11-tetrahydronaphtho[2,3-g]quinolinium perchlorate |
| Purity | ≥90% (coupling to thiols) |
| IUPAC Name | 4-[9-(dimethylamino)-11,11-dimethyl-3,4-dihydro-2H-naphtho[2,3-g]quinolin-1-ium-1-yl]-N-[2-(2,5-dioxopyrrol-1-yl)ethyl]butanamide;perchlorate |
| SMILES | CC1(C2=CC3=[N+](CCCC3=CC2=CC4=C1C=C(C=C4)N(C)C)CCCC(=O)NCCN5C(=O)C=CC5=O)C.[O-]Cl(=O)(=O)=O |
| InChI | InChI=1S/C31H36N4O3.ClHO4/c1-31(2)25-19-24(33(3)4)10-9-21(25)17-23-18-22-7-5-14-34(27(22)20-26(23)31)15-6-8-28(36)32-13-16-35-29(37)11-12-30(35)38;2-1(3,4)5/h9-12,17-20H,5-8,13-16H2,1-4H3;(H,2,3,4,5) |
| InChIKey | NIZBDUMEZAIMFT-UHFFFAOYSA-N |
| MDL Number | MFCD04040681 |
| NACRES | NA.32 |
Product Specification
| Excitation | 610 |
| Emission | 637 |
| Properties Quality Level | 100 |
| Storage | −20 °C |
Application
ATTO 610 maleimide is a thiol-reactive fluorescent labeling reagent built on the ATTO 610 fluorophore, designed for efficient conjugation to cysteine-containing biomolecules via maleimide-thiol coupling. Its red/orange emission makes it a widely used component in fluorescence microscopy, flow cytometry, and fluorescence-based bioconjugation workflows where bright, dye-tagged conjugates are needed for imaging and quantification.
1. Protein And Peptide Labeling
ATTO 610 maleimide is frequently used to prepare fluorescent protein and peptide conjugates for biochemical assays and molecular imaging studies. Researchers label purified proteins, antibody fragments, enzyme variants, and engineered peptides that contain accessible cysteine residues, enabling direct visualization of binding, localization, and trafficking in experimental systems. The maleimide functional group supports straightforward dye incorporation into thiol-bearing targets, producing stable dye-tagged conjugates that are commonly used as labeling standards for assay development and method validation.
2. Fluorescence Microscopy Staining
ATTO 610 maleimide is well suited for fluorescence microscopy workflows that require red/orange channel imaging of cysteine-labeled biomolecules. In cell biology and chemical biology laboratories, it is used to generate fluorescent conjugates for staining experiments such as tracking protein interactions at the cell surface, monitoring receptor-associated components, and visualizing labeled ligands during uptake or binding assays. The ATTO 610 emission profile supports multiplexing with other fluorophores by providing a distinct spectral window, which is particularly useful when designing multi-color imaging panels.
3. Flow Cytometry Conjugates
ATTO 610 maleimide is commonly employed to generate flow cytometry dyes for labeling cells with thiol-reactive fluorescent conjugates. Researchers use it to tag cell-binding reagents, such as cysteine-containing targeting ligands or engineered binding proteins, followed by incubation with cells to quantify binding by fluorescence readout. This approach supports routine development of fluorescence-based binding assays and phenotyping workflows where consistent labeling of thiol-containing components is required for reproducible signal generation across samples.
4. Biomaterial Surface Functionalization
ATTO 610 maleimide is used in biomaterials science to fluorescently functionalize surfaces and constructs that present accessible thiol groups. Material developers incorporate ATTO 610 dye into thiol-bearing polymers, hydrogel networks, or surface coatings to create fluorescently traceable materials for microscopy-based characterization, coating uniformity checks, and spatial mapping of biomolecule immobilization. Such labeled materials are also used in platform screening to evaluate how surface chemistry influences biomolecule attachment and subsequent assay readouts.
Computed Properties
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 8 |
| Rotatable Bond Count | 8 |
| Exact Mass | 612.2350772 g/mol |
| Monoisotopic Mass | 612.2350772 g/mol |
| Topological Polar Surface Area | 147Ų |
| Heavy Atom Count | 43 |
| Formal Charge | 0 |
| Complexity | 1250 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently-Bonded Unit Count | 2 |
| Compound Is Canonicalized | Yes |
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