
Rhodamine 110, bis-(CBZ-L-alanyl-L-alanyl-L-alanyl-L-alanine amide)
| Catalog Number | A18-0090 |
| Category | Fluorescent Enzyme Substrates |
| Molecular Formula | C60H66N10O15 |
| Molecular Weight | 1167.24 |
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Product Introduction
Rhodamine 110, bis-(CBZ-L-alanyl-L-alanyl-L-alanyl-L-alanine amide) is a peptide-based fluorescent dye featuring the xanthene chromophore class, known for its vibrant green fluorescence upon excitation. This compound contains a bisamide linkage that enables its use in bioimaging applications, particularly in protease activity assays where enzymatic cleavage releases the fluorescent rhodamine moiety. The molecule's design facilitates its incorporation into fluorescence microscopy workflows, allowing researchers to monitor and visualize proteolytic processes in real-time.
Chemical Information
Application
Chemical Information
| Synonyms | R 110, 2(AAAA)amide; Rh 110, 2(Ala-Ala-Ala-Ala)Amide |
Application
Rhodamine 110, bis-(CBZ-L-alanyl-L-alanyl-L-alanyl-L-alanine amide) is a rhodamine 110-based, peptide-amide conjugate designed for fluorescence readouts in chemical biology workflows. The rhodamine 110 scaffold provides strong visible fluorescence suitable for imaging and assay development, while the multi-alanine amide architecture supports incorporation into protease- and peptide-processing studies and peptide-linked probe constructs. In practice, it is used as a fluorescent reporting reagent where peptide structure and rhodamine emission together enable monitoring of enzymatic or processing events in solution and in biomolecular labeling contexts.
1. Protease Activity Reporting
Rhodamine 110, bis-(CBZ-L-alanyl-L-alanyl-L-alanyl-L-alanine amide) is used as a fluorescence reporting reagent in protease activity assays that rely on peptide-bond processing to generate a measurable change in rhodamine emission. Researchers commonly employ it in microplate fluorescence formats to compare enzyme activity across conditions such as buffer composition, time course, and inhibitor screening for protease classes that act on peptide substrates. The peptide-amide design supports construction of peptide-linked assay reagents, enabling signal readout in aqueous assay systems compatible with standard fluorescence readers.
2. Peptide-Linked Probe Construction
Rhodamine 110, bis-(CBZ-L-alanyl-L-alanyl-L-alanyl-L-alanine amide) serves as a building-block fluorophore for constructing peptide-based fluorescent probes used in chemical biology. Teams developing substrate analogs for enzymatic studies or fluorescent peptide conjugates incorporate this reagent into larger probe architectures where rhodamine emission provides the optical readout, and the peptide motif supports recognition by peptide-processing enzymes or incorporation into peptide assemblies. This approach is frequently used to generate tunable fluorescent tools for monitoring biomolecular processing events in solution-phase assays and imaging experiments.
3. Fluorescence Microscopy Staining Reagents
Rhodamine 110, bis-(CBZ-L-alanyl-L-alanyl-L-alanyl-L-alanine amide) is used as a rhodamine-emitting staining reagent in fluorescence microscopy workflows where peptide-linked fluorescent signals are tracked in fixed samples or in controlled labeling experiments. Research groups use rhodamine fluorescence to visualize spatial distribution of fluorescently labeled peptide constructs and to follow processing-dependent signal changes in microscopy studies. The dye's bright visible emission supports imaging on common epifluorescence and fluorescence microscope platforms, facilitating qualitative localization and comparative imaging across experimental conditions.
4. Biomolecular Labeling Studies
Rhodamine 110, bis-(CBZ-L-alanyl-L-alanyl-L-alanyl-L-alanine amide) is applied in biomolecular labeling and fluorescence-tagging studies where a rhodamine 110 fluorophore is coupled to a peptide-amide framework to create a fluorescent conjugate for monitoring labeling outcomes. Chemical biology and materials researchers use it to track conjugate formation, processing, or release in peptide-containing systems, including fluorescence-based characterization of labeled biomolecules. The resulting rhodamine fluorescence provides a convenient optical handle for verifying incorporation and for monitoring changes during sample preparation and assay execution.
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