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Product Introduction
ATTO 633 belongs to a new generation of fluorescent labels for the red spectral region. The dye is designed for application in the area of life science, e.g. labelling of DNA, RNA or proteins. Characteristic features of the label are strong absorption, high fluorescence quantum yield, high photostability, good water solubility, and very little triplet formation. ATTO 633 is a cationic dye. After coupling to a substrate the dye carries a netelectrical charge of +1. In common with most ATTO-labels, absorption and fluorescence are independent of pH, at least in the range of pH 2 to 11, used in typical applications.The iodoacetamide derivative reacts, like the maleimide, with a sulfhydryl group forming a thioether bond. It is predominantly used for tagging cystein residues of proteins.find more information here
Chemical Information
Application
Chemical Information
| NACRES | NA.32 |
Application
ATTO 633 iodoacetamide is a thiol-reactive ATTO 633 fluorophore conjugate designed for fluorescent labeling of cysteine-containing biomolecules via alkylation of sulfhydryl groups. With far-red emission for low-background imaging workflows, it is commonly used to generate stable fluorescent conjugates for protein labeling, probe construction, and quantitative fluorescence assays where controlled dye-to-biomolecule attachment is required.
1. Protein Thiol Labeling
ATTO 633 iodoacetamide is widely used in protein labeling workflows where accessible cysteine residues are available for site-specific or semi-selective fluorescent tagging. Researchers apply it to label purified proteins, enzymes, and affinity reagents to enable fluorescence microscopy, fluorescence-based binding studies, and quantitative readouts in microplate formats. The iodoacetamide functionality drives efficient covalent attachment to thiols, producing conjugates that remain fluorescent under typical labeling and wash steps used in biochemical characterization and imaging experiments.
2. Fluorescent Probe Construction
ATTO 633 iodoacetamide serves as a practical dye-building block for constructing fluorescent probes and labeling reagents that require far-red emission. Chemical biology and materials researchers incorporate it into antibody fragments, peptides, and other thiol-bearing targeting ligands to produce imaging reagents for localization studies and assay development. Because the dye is installed through covalent thiol chemistry, conjugates are often used when stable labeling is preferred over noncovalent dyes, including workflows that involve repeated washing, immobilization, or conjugate handling during probe optimization.
3. Biomolecule Conjugate Tracking
ATTO 633 iodoacetamide is frequently employed to generate fluorescent conjugates for tracking biomolecule distribution and interactions in solution and on surfaces. In bioconjugation and biomaterials research, labeled proteins and peptides prepared with this reagent are used as fluorescent tracers to monitor binding, immobilization efficiency, and transport in assay and materials development settings. The far-red ATTO 633 signal supports imaging and quantification in multi-component experimental systems where spectral separation from common green/yellow fluorophores is advantageous.
4. Flow Cytometry Labeling
ATTO 633 iodoacetamide is used to label thiol-containing biomolecules for flow cytometry experiments that benefit from far-red detection channels. Researchers prepare fluorescent conjugates for staining workflows such as labeling of antibodies or protein-based binders that contain reactive cysteines, enabling readouts of binding to cell-associated targets or assay reagents. Covalent thiol labeling helps maintain dye attachment through staining and washing steps, supporting reproducible fluorescence measurements during instrument-based analysis.
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