
CBQCA Reagent | CAS 131124-59-9
| Catalog Number | F02-0043 |
| Category | Other Cyanine |
| Molecular Formula | C18H11NO4 |
| Molecular Weight | 305.29 |
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Product Introduction
High-sensitivity fluorescent assay reagent for protein and peptide quantification. Forms stable fluorescent adducts for spectroscopic analysis.
Chemical Information
Product Specification
Application
Chemical Information
| Synonyms | CBQCA;3-(4-Carboxybenzoyl)-2-quinolinecarboxaldehyde; 3-(4-Carboxybenzoyl)quinoline-2-carboxaldehyde; 4-[(2-formylquinolin-3-yl)carbonyl]benzoic acid |
| SMILES | C1=CC=C2C(=C1)C=C(C(=N2)C=O)C(=O)C3=CC=C(C=C3)C(=O)O |
| InChI | InChI=1S/C18H11NO4/c20-10-16-14(9-13-3-1-2-4-15(13)19-16)17(21)11-5-7-12(8-6-11)18(22)23/h1-10H,(H,22,23) |
| InChIKey | MWNLTKCQHFZFHN-UHFFFAOYSA-N |
Product Specification
| Excitation | 465 |
| Emission | 558 |
| Storage | 24 months after receival at -20°C in the dark. Transportation: at room temperature for up to 3 weeks. Avoid prolonged exposure to light. |
Application
CBQCA Reagent is a fluorescent labeling reagent used to quantify primary amines in proteins and peptides through formation of a highly fluorescent adduct. In routine fluorescence-based assays, it enables sensitive readout of biomolecule concentration in microplate formats, supporting workflows in protein chemistry, analytical bioconjugation, and biomaterials characterization where direct UV/Vis quantitation is insufficient. The reagent's amine-reactive chemistry and strong fluorescence response make it a common choice for monitoring labeling efficiency and sample-to-sample normalization in research-grade assays.
1. Protein Concentration Assays
CBQCA Reagent is frequently used to determine protein concentration in research laboratories by converting primary amine groups into a fluorescent product compatible with standard fluorescence plate readers. Researchers in proteomics sample preparation, protein purification, and analytical biochemistry rely on this approach to quantify protein yields from fractions, compare buffer-exchange outcomes, and normalize inputs for downstream experiments such as SDS-PAGE densitometry cross-checks or immunoassay setup. Because the readout is fluorescence-based, it is often selected when samples contain components that interfere with absorbance measurements.
2. Peptide And Amine Quantification
CBQCA Reagent also supports quantification of peptides and other primary-amine-containing analytes, enabling researchers to track peptide recovery after purification steps and to assess relative amounts of amine-bearing building blocks used in chemical biology and medicinal chemistry workflows. In peptide synthesis development and scale-up, it is commonly used as a rapid orthogonal measurement to estimate material losses during workup and purification. The fluorescence readout provides a convenient way to compare batches and to standardize concentrations before conjugation, immobilization, or assay incorporation.
3. Bioconjugation Reaction Monitoring
CBQCA Reagent is widely applied to monitor bioconjugation and labeling workflows in which primary amines are modified, such as amine-directed coupling strategies used to generate protein conjugates, surface-functionalized biomaterials, or fluorescent labeling intermediates. By measuring changes in available amine content before and after reaction steps, researchers can estimate labeling extent and guide optimization of reagent ratios or reaction conditions in iterative development. This use case is particularly common in laboratories building fluorescent conjugates for molecular imaging reagent development, where consistent labeling levels are needed for reproducible fluorescence readouts.
4. Biomaterial And Surface Functionalization
CBQCA Reagent is employed in biomaterials science to evaluate functionalization of amine-containing surfaces and coatings, including polymer films, hydrogel materials, and immobilized biomolecule layers. Researchers use the fluorescent amine assay to quantify the extent of surface modification and to compare functional group densities across fabrication batches. In addition to material characterization, this approach helps ensure consistent starting chemistry for subsequent steps such as affinity reagent immobilization, linker installation, or preparation of assay-ready functional surfaces.
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