Cy3 carboxylic acid (non-sulfonated)

Cy3 carboxylic acid (non-sulfonated)

Catalog Number:
DAD1368208APE
Mfr. No.:
APE-A8132
Price:
$392
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      • Overview
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          Background

          Cy3 carboxylic acid is a non-activated fluorescence dye. Most derivatives of non-sulfonated cyanines have low aqueous solubility except for hydrochlorides of hydrazides and amines. This Non-sulfonated reagent has limited aqueous solubility, but with good solubility in organic solvents. For biomolecule labeling, the labeling reagent has low aqueous solubility, using of organic co-solvent to dissolve this molecular is necessary for efficient reaction. First, Cyanine dye should be dissolved in organic solvent and then added to a solution of biomolecule in appropriate aqueous buffer. In the supramolecular glutamine assay, Cy3 carboxylic acid was conjugated to a single strain DNA and then immobilized onto the glass slide through DNA hybridization. The Cy3 groups serve as FRET donor and the cyclodextrins as supramolecular host [1].

          Reference: [1] Xue, M. ; Wei, W.; Su, Y.; Johnson, D.; Heath, J.R. Supramolecular Probes for Assessing Glutamine Uptake Enable Semi-Quantitative Metabolic Models in Single Cells. Journal of the American Chemical Society, 2016, 138(9), 3085–3093.

      • Properties
        • Categories
          Non-reactive fluorophore, for control experiments, and for calibration
          Alternative Name
          1-(5-carboxypentyl)-3,3-dimethyl-2-((1E,3E)-3-(1,3,3-trimethylindolin-2-ylidene)prop-1-en-1-yl)-3H-indol-1-ium chloride
          Molecular Formula
          C30H37ClN2O2
          Molecular Weight
          493.08
          Appearance
          A solid
          Purity
          98.00%
          Solubility
          ≥49.3 mg/mL in DMSO; insoluble in H2O; ≥99 mg/mL in EtOH
          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. Desiccate.
          SMILES
          CC(C1=C(N/2C)C=CC=C1)(C)C2=C/C=C/C3=[N+](CCCCCC(O)=O)C(C=CC=C4)=C4C3(C)C.[Cl-]

          * For Research Use Only

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