
5-(6)-Carboxy SNAFL-1 SE
| Catalog Number | A15-0012 |
| Category | pH Indicators |
| Molecular Formula | C29H17NO9 |
| Molecular Weight | 523.45 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
An amine-reactive succinimidyl ester pH indicator with dual-emission ratiometry. Ideal for labeling proteins and cellular compartments for quantitative pH imaging.
Product Specification
Application
Product Specification
| Excitation | 490 |
| Emission | 513 |
Application
5-(6)-Carboxy SNAFL-1 SE is a SE-reactive, carboxylated fluorescein-based dye designed for covalent fluorescent labeling in biological workflows. Its succinimidyl ester functionality enables efficient conjugation to primary amines on proteins, peptides, and other amine-containing biomolecules, while the carboxyl group supports downstream handling in labeling and imaging reagent development. The fluorescein spectral profile is commonly leveraged in fluorescence microscopy and fluorescence-based bioassays where green emission readouts are required.
1. Protein And Peptide Labeling
5-(6)-Carboxy SNAFL-1 SE is used by protein chemistry and chemical biology groups to generate amine-labeled fluorescent conjugates for imaging and assay development. Researchers typically attach the dye to antibodies, enzyme proteins, receptor ligands, or peptide probes to create fluorescent reagents for binding studies, workflow validation, and fluorescent tracking of biomolecule distribution in experimental systems. The SE ester chemistry supports straightforward conjugate preparation for downstream use in fluorescence microscopy and plate-based fluorescence assays, where fluorescein emission is routinely monitored.
2. Fluorescence Microscopy Staining
5-(6)-Carboxy SNAFL-1 SE supports fluorescence microscopy experiments where amine-reactive labeling of fixed biological samples or labeled biomolecule components is needed. Molecular imaging teams use the dye to visualize fluorescently tagged proteins on cellular surfaces, in extracellular matrices, or within labeled biomolecular constructs, enabling localization studies with green-channel detection. The carboxylated fluorescein scaffold also helps maintain practical conjugate compatibility for multistep staining workflows that require stable, covalently attached fluorescent labels.
3. Fluorescence Bioassay Reagent Development
5-(6)-Carboxy SNAFL-1 SE is frequently incorporated into fluorescence assay development for generating labeled assay components such as fluorescent substrates, detection reagents, or tracer molecules. Assay developers use the dye-conjugated biomolecules to monitor binding events, reagent uptake, or assay readouts in fluorescence plate formats where fluorescein emission is convenient for standard instrumentation. Covalent labeling helps ensure the fluorescent signal remains associated with the intended biomolecular reagent during washing and incubation steps common to fluorescence-based screening and characterization workflows.
4. Flow Cytometry Conjugate Preparation
5-(6)-Carboxy SNAFL-1 SE is used to prepare fluorescein-channel flow cytometry reagents by covalently labeling amine-containing targeting proteins such as antibodies or affinity reagents. Cytometry users rely on the dye's SE reactivity to generate consistent fluorescent conjugates for staining panels and instrument-based quantification of labeled binding to cells or cell-associated biomolecules in research assays. The carboxylated fluorescein motif supports routine handling of fluorescent conjugates in staining workflows that require stable covalent attachment prior to analysis.
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