Sulfo-Cy3-Amide-C6-Amine
Catalog Number | F03-0027 |
Category | sulfo-Cyanine3 |
Molecular Formula | C38H52N4Na2O10S3 |
Molecular Weight | 867.0 |
Catalog Number | Size | Price | Quantity |
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F03-0027 | -- | $-- |
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Product Introduction
Sulfo-Cy3-Amide-C6-Amine is a water-soluble dye. The amine group can react with carboxylic acids, activated NHS esters, carbonyls (ketone, aldehyde) etc.
Chemical Information |
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Purity | 98% |
IUPAC Name | disodium;(2E)-1-[6-(6-aminohexylamino)-6-oxohexyl]-2-[(E)-3-[3,3-dimethyl-5-sulfonato-1-(3-sulfonatopropyl)indol-1-ium-2-yl]prop-2-enylidene]-3,3-dimethylindole-5-sulfonate |
Canonical SMILES | CC1(C2=C(C=CC(=C2)S(=O)(=O)[O-])[N+](=C1C=CC=C3C(C4=C(N3CCCCCC(=O)NCCCCCCN)C=CC(=C4)S(=O)(=O)[O-])(C)C)CCCS(=O)(=O)[O-])C.[Na+].[Na+] |
InChI | InChI=1S/C38H54N4O10S3.2Na/c1-37(2)30-26-28(54(47,48)49)17-19-32(30)41(23-11-7-8-16-36(43)40-22-10-6-5-9-21-39)34(37)14-12-15-35-38(3,4)31-27-29(55(50,51)52)18-20-33(31)42(35)24-13-25-53(44,45)46;;/h12,14-15,17-20,26-27H,5-11,13,16,21-25,39H2,1-4H3,(H3-,40,43,44,45,46,47,48,49,50,51,52);;/q;2*+1/p-2 |
InChI Key | HCHYMTGLKRSLLE-UHFFFAOYSA-L |
- Product Specification
- Application
Storage | -20 °C |
Sulfo-Cy3-Amide-C6-Amine is a fluorescent dye that is part of the cyanine group, known for its vivid orange-red fluorescence. This compound features a sulfonic acid group, which enhances its solubility in aqueous solutions, making it particularly useful in biological applications. The amide linkage and the C6 spacer provide a stable connection and flexibility, allowing it to be conjugated easily to a variety of biomolecules such as proteins, antibodies, and peptides. This adaptability furthers its appeal in complex biological systems. The presence of an amine group enables attachment to different functional groups, making it an essential tool in diversifying its use across biochemical and cellular imaging applications.
One of the primary applications of Sulfo-Cy3-Amide-C6-Amine is in fluorescence microscopy. Its bright fluorescence and high photo-stability make it ideal for labeling and visualizing cellular components. When conjugated to antibodies, it allows for the precise localization of proteins within a cell, aiding in the understanding of cellular processes and the identification of disease markers. This application is crucial for both research and diagnostic purposes, where high-resolution and specific imaging are required. The superior water solubility attributed to its sulfonic acid group also ensures that it performs well in live-cell imaging, maintaining cell viability while providing clear and bright images.
Another significant application of Sulfo-Cy3-Amide-C6-Amine is in flow cytometry. This technique requires the use of fluorescent dyes that can bind specifically to cellular markers and provide quantitative information about cell populations. Sulfo-Cy3-Amide-C6-Amine’s compatibility with other fluorescent dyes allows it to be used in multi-color assays, enabling the analysis of multiple parameters simultaneously. Its high fluorescence output and stability facilitate accurate detection and quantification of target molecules in a population of cells, making it indispensable for applications such as immunophenotyping, cell sorting, and biomarker discovery, enhancing the overall capabilities of flow cytometry.
Additionally, Sulfo-Cy3-Amide-C6-Amine is used in the development of fluorescent assays for biomolecule interactions. By labeling ligands, peptides, or small molecules, researchers can monitor interactions through fluorescence resonance energy transfer (FRET) or other fluorescence-based techniques. This application is especially important in drug discovery and development, where understanding the interactions of potential therapeutic agents with targets can guide the design of more effective and selective drugs. Its ability to conjugate readily with diverse biomolecules makes it a versatile tool in tracking binding events and mapping out interaction networks.
Finally, Sulfo-Cy3-Amide-C6-Amine is employed in the creation of biosensors. Biosensors designed for detecting various analytes, such as nucleic acids or small molecules, benefit greatly from the high sensitivity and specificity provided by this dye. It can be used to monitor changes in fluorescence intensity as a response to the presence of the target analyte, allowing for real-time and non-invasive detection. This capability is particularly beneficial in clinical diagnostics and environmental monitoring, where rapid and accurate sensor readouts are required. The adaptability and robust performance of Sulfo-Cy3-Amide-C6-Amine in these applications underline its importance in expanding the functional scope of biosensing technologies.
Computed Properties | |
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Hydrogen Bond Donor Count | 2 |
Hydrogen Bond Acceptor Count | 12 |
Rotatable Bond Count | 19 |
Exact Mass | 866.26409595 g/mol |
Monoisotopic Mass | 866.26409595 g/mol |
Topological Polar Surface Area | 258Ų |
Heavy Atom Count | 57 |
Formal Charge | 0 |
Complexity | 1760 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 0 |
Undefined Atom Stereocenter Count | 0 |
Defined Bond Stereocenter Count | 2 |
Undefined Bond Stereocenter Count | 0 |
Covalently-Bonded Unit Count | 3 |
Compound Is Canonicalized | Yes |
Applications of Fluorescent Probes & Dyes
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