
JOE NHS ester, 5-isomer | CAS 113394-24-4
| Catalog Number | F12-0002 |
| Category | JOE Dyes |
| Molecular Formula | C27H17Cl2NO11 |
| Molecular Weight | 602.33 |
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Product Introduction
JOE NHS ester, 5-isomer is an activated N-hydroxysuccinimide ester used to label proteins, peptides, amino-modified oligonucleotides, and other target molecules via conjugation with amines.
Chemical Information
Product Specification
Application
Chemical Information
| Appearance | Orange Powder |
Product Specification
| Excitation | 533 |
| Emission | 554 |
Application
NHS ester derivatives are widely used protein bioconjugation reagents for installing stable amide linkages onto primary amine groups under standard aqueous labeling conditions. JOE NHS ester, 5-isomer provides a reactive N-hydroxysuccinimide ester handle for coupling to lysine residues on proteins, peptides, and other amine-containing biomolecules, enabling fluorescent labeling for downstream imaging and fluorescence-based assays. Its use in conjugate preparation supports consistent reagent workflows in molecular biology, chemical biology, and microscopy/flow cytometry development.
1. Protein Fluorescent Labeling
JOE NHS ester, 5-isomer is commonly employed by researchers to generate fluorescently labeled proteins for fluorescence microscopy, fluorescence imaging workflows, and assay development where amine-reactive labeling is required. By coupling to lysine side chains and N-terminal amines, the reagent enables preparation of labeled antibodies, enzymes, affinity proteins, and protein standards used to track binding, localization, and biomolecular interactions in solution or on surfaces. Conjugates prepared from this NHS-ester chemistry are also frequently used as reference reagents in fluorescence-based characterization experiments, including labeling stoichiometry optimization and method development for imaging and detection platforms.
2. Antibody Conjugate Preparation
JOE NHS ester, 5-isomer supports fluorescent antibody conjugate construction for immunofluorescence and fluorescence-based binding assays that rely on robust covalent attachment to antibody amines. Chemical biology and diagnostic-reagent development teams often use NHS ester labeling to produce labeled secondary antibodies, detection antibodies, and antibody fragments for microscopy readouts and plate-based fluorescence assays. This labeling approach is particularly useful when a stable dye-biomolecule conjugate is needed for repeated washing steps, multistep assay workflows, or comparative studies across antibody lots, since amide bond formation provides durable attachment compared with noncovalent dye association.
3. Peptide And Biomolecule Tagging
JOE NHS ester, 5-isomer is frequently used to fluorescently tag peptides and other amine-containing biomolecules to enable tracking in biochemical assays and molecular imaging experiments. Investigators use this reagent to prepare labeled substrates, binding partners, or tracer molecules for monitoring interactions, distribution, and kinetics in fluorescence readouts. In biomaterials and surface science workflows, dye-labeled peptides and protein fragments prepared via NHS ester coupling are also used to create fluorescent probes for studying adsorption, immobilization behavior, and biomolecule presentation on engineered materials.
4. Flow Cytometry Labeling Reagents
JOE NHS ester, 5-isomer is used to produce fluorescence labeling reagents for flow cytometry workflows where covalent dye attachment to protein targets supports consistent staining across experimental runs. Researchers commonly prepare labeled antibodies or protein reagents for cell-surface or extracellular labeling strategies, followed by flow-based readout of fluorescence intensity distributions. This NHS-ester labeling strategy is also used in assay development for optimizing staining panels, generating fluorescence standards, and preparing conjugates for instrument verification and gating strategy development in fluorescence-quantification experiments.
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