1481447-40-8
Chemical Structure
Sulfo-Cy5-N3
- CAS No.: 1481447-40-8
- Formula:C35H44N6O7S2
- Molecular Weight:724.89
IUPAC Name: tert-butyl ((5-chlorothiophen-2-yl)methyl)glycinate
InChIKey: FKUPPCIOTWHEDE-UHFFFAOYSA-N
SMILES: O=S(C1=CC2=C([N+](C)=C(C=CC=CC=C3N(CCCCCC(NCCCN=[N+]=[N-])=O)C4=C(C=C(S(=O)(O)=O)C=C4)C3(C)C)C2(C)C)C=C1)([O-])=O
Biological Activity: Sulfo-Cy5-N3 is an azide-functionalized sulfonated cyanine 5 Fluorescent dye and also serves as click chemistry coupling reagent. Sulfo-Cy5-N3 undergoes copper (I)-catalyzed azide-alkyne cycloaddition with alkyne-functionalized antibody constructs and peptide probes for site-selective fluorescent labeling. Sulfo-Cy5-N3 also acts as an emission dye for STORM super-resolution imaging. Sulfo-Cy5-N3 is applicable to the study of HER2-positive breast cancer[1][2].
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Sulfo-Cy5-N3 | 98.88% | Sulfo-Cy5-N3 is an azide-functionalized sulfonated cyanine 5 Fluorescent dye and also serves as click chemistry coupling reagent. Sulfo-Cy5-N3 undergoes copper (I)-catalyzed azide-alkyne cycloaddition with alkyne-functionalized antibody constructs and peptide probes for site-selective fluorescent labeling. Sulfo-Cy5-N3 also acts as an emission dye for STORM super-resolution imaging. Sulfo-Cy5-N3 is applicable to the study of HER2-positive breast cancer. | ||||||||||||||||||||
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