MW 351.5 Da, Purity >98%. Fluorescent probe for measuring protein conformational changes and quantitative measurement of protein hydrophobicity processes that modify the exposure of the probe to water. Essentially nonfluorescent in water. Fluorescent when bound to membranes (q.y. ~0.27) or hydrophobic domains of proteins (q.y. ~0.72). Fluorescence enhanced by cyclodextrins. Can be used to provide a sensitive method for separating and analyzing cyclodextrins by capillary electrophoresis.
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- Archives of biochemistry and biophysics 474:198-2042008Spectral resolution of a second binding site for Nile Red on cytochrome P4503A4.Applications:Unspecified applicationReactive species:Unspecified reactive speciesAbhinav Nath et. al.PubMed 18395506
- Biochemistry 47:509-162007Nile Red is a fluorescent allosteric substrate of cytochrome P450 3A4.Applications:Unspecified applicationReactive species:Unspecified reactive speciesJed N Lampe,Cristina Fernandez,Abhinav Nath,William M AtkinsPubMed 18092806
Key facts
- CAS number
- 32752-10-6
- Purity
- > 98%
- Form
- Solid
- Molecular weight
- 351.5 Da
- Molecular formula
- C17H14KNO3S
- PubChem identifier
- 23666335
- Nature
- Synthetic
- Excitation/Emission
- Ex: 318nm, Em: 443nm
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MW 351.5 Da, Purity >98%. Fluorescent probe for measuring protein conformational changes and quantitative measurement of protein hydrophobicity processes that modify the exposure of the probe to water. Essentially nonfluorescent in water. Fluorescent when bound to membranes (q.y. ~0.27) or hydrophobic domains of proteins (q.y. ~0.72). Fluorescence enhanced by cyclodextrins. Can be used to provide a sensitive method for separating and analyzing cyclodextrins by capillary electrophoresis.
Key facts
- CAS number
- 32752-10-6
- Purity
- > 98%
- Form
- Solid
- Molecular weight
- 351.5 Da
- Molecular formula
- C17H14KNO3S
- PubChem identifier
- 23666335
- Nature
- Synthetic
- Solubility
Soluble in DMSO.
Soluble in water.
- Biochemical name
- Potassium 6-(p-toluidino)naphthalene-2-sulphonate
- Biological description
Fluorescent probe for measuring protein conformational changes and quantitative measurement of protein hydrophobicity processes that modify the exposure of the probe to water. Essentially nonfluorescent in water. Fluorescent when bound to membranes (q.y. ~0.27) or hydrophobic domains of proteins (q.y. ~0.72). Fluorescence enhanced by cyclodextrins. Can be used to provide a sensitive method for separating and analyzing cyclodextrins by capillary electrophoresis.
- Canonical SMILES
- CC1=CC=C(C=C1)NC2=CC3=C(C=C2)C=C(C=C3)S(=O)(=O)[O-].[K+]
- InChI
- InChI=1S/C17H15NO3S.K/c1-12-2-6-15(7-3-12)18-16-8-4-14-11-17(22(19,20)21)9-5-13(14)10-16;/h2-11,18H,1H3,(H,19,20,21);/q;+1/p-1
- InChIKey
- GVDCHDBOXJUSDZ-UHFFFAOYSA-M
- IUPAC name
- potassium;6-(4-methylanilino)naphthalene-2-sulfonate
- Excitation/Emission
- Ex: 318nm, Em: 443nm
Storage
- Shipped at conditions
- Blue Ice
- Appropriate short-term storage conditions
- +4°C
- Appropriate long-term storage conditions
- +4°C
- Storage information
- Store in the dark, Store under desiccating conditions
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1 product image
Chemical Structure - 6-p-Toluidino-2-naphthalenesulfonic acid, potassium salt (TNS-K+) (ab275213)
Chemical structure of 6-p-Toluidino-2-naphthalenesulfonic acid, potassium salt (TNS-K+), 32752-10-6
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