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Merck

10417

Sigma-Aldrich

8-Anilino-1-naphthalenesulfonic acid ammonium salt

for fluorescence, ≥97.0% (HPLC)

Szinonimák:

1,8-ANS NH4, ANSA, Ammonium 8-anilino-1-naphthalenesulfonate, N-Phenyl peri acid

Bejelentkezésa Szervezeti és Szerződéses árazás megtekintéséhez


About This Item

Lineáris képlet:
C16H13NO3S · NH3
CAS-szám:
Molekulatömeg:
316.37
Beilstein:
3581235
EC-szám:
MDL-szám:
UNSPSC kód:
12352106
PubChem Substance ID:
NACRES:
NA.32
Forma:
solid
Teszt:
≥97.0% (HPLC)

grade

for fluorescence

Minőségi szint

Teszt

≥97.0% (HPLC)

Forma

solid

veszteség

≤2.5% loss on drying

mp

245-253 °C

oldhatóság

H2O: 0.1 g/5mL, clear to very slightly hazy (hot)
NaOH: 1 N
H2O: soluble
acetone: soluble
methanol: soluble

fluoreszcencia

λex 388 nm; λem 470 nm in 0.1 M Tris, 0.2 M KCl, pH 9.0, BSA

SMILES string

N.OS(=O)(=O)c1cccc2cccc(Nc3ccccc3)c12

InChI

1S/C16H13NO3S.H3N/c18-21(19,20)15-11-5-7-12-6-4-10-14(16(12)15)17-13-8-2-1-3-9-13;/h1-11,17H,(H,18,19,20);1H3

Nemzetközi kémiai azonosító kulcs

IPBNQYLKHUNLQE-UHFFFAOYSA-N

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Alkalmazás

ANS forms an inclusion complex with cyclodextrin. Such model systems are useful to mimic biological recognition and can be studied by measuring the change in fluorescence of free-ANS to complexed-ANS. When ANS enters the hydrophobic core of cyclodestrin, it′s fluorescence increases . Utilized in the reagent phase of a sodium-selective fiber-optic sensor. The reagent phase also contains a copper(II) polyelectrolyte, which binds to ANSA in the absence of sodium and quenches the fluorescence. In the presence of sodium, ANSA forms a cationic complex creating ion-pairs, causing it to fluoresce . ANS is often incorporated into di-block polymers and can be released by changes in the local environment (i.e., temperature, pH, etc.) . ANS is commonly used as a fluorescence probe to investigate molecular assemblies of surfactants and amphiphilic polymers because a blue shift of the emission maximum indicates the fluorophore is located in less polar media . Fluorescent probe for protein studies using methodologies such as steady-state and dynamic fluorescence measurements .
This product is an amphiphilic fluorescent probe for protein studies . Excitation of the unbound dye at 380 nm results in a low fluorescent emission with a maximum at 545 nm. The fluorescence intensity of ANS increases when the dye binds to the hydrophobic regions of a protein . The protein-ANS complex has an emission spectrum which is shifted to a broad maximum at 470 nm. At pH 8, protein causes a 40-fold increase in the relative quantum yield compared to free ANS in solution . ANS has been used to monitor protein conformational changes by binding to the hydrophobic regions of a protein , to gain new insight into protein binding interactions, often by acting as reporter or competitor ligands, to investigate the visual excitation process and structural aspects of photoreceptor cell membranes , and to probe (and disrupt) the structure of both high- and low-density lipoproteins. It has also been used as a substrate in a chemiluminescent enzyme immunoassay system and as a dye for yeast viability determination. The conformational states for apo- and holo- yeast alcohol dehydrogenase were reported under conditions of low pH using ANS fluorescence . ANS is also commonly used as a fluorescence probe to investigate molecular assemblies of surfactants and amphiphilic polymers because a blue shift of its emission maximum indicates the probe is located in less polar environment

Tárolási osztály kódja

11 - Combustible Solids

WGK

WGK 3

Lobbanási pont (F)

Not applicable

Lobbanási pont (C)

Not applicable

Egyéni védőeszköz

dust mask type N95 (US), Eyeshields, Gloves


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Analitikai tanúsítványok (COA)

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Dokumentumtár megtekintése

Az ügyfelek ezeket is megtekintették

Evaluation of the fluorescent dye 1-anilino-8-naphtahalene sulfonic acid for yeast viability determination
McCaig, R.
Journal of the American Society of Brewing Chemists, 48, 22-22 (1990)
Quantitative estimation of protein binding site polarity. Fluorescence of N-arylaminonaphthalenesulfonates.
D C Turner et al.
Biochemistry, 7(10), 3381-3390 (1968-10-01)
Monitoring protein conformational changes during membrane fusion.
T Yoshimura
Methods in enzymology, 221, 72-82 (1993-01-01)
Hydrophobic domain structure of water-soluble block copolymer. 2. Transition phenomena of block copolymer micelles
Ikemi, M., et al.
Macromolecules, 15, 15-15 (1982)
The interaction of a naphthalene dye with apomyoglobin and apohemoglobin. A fluorescent probe of non-polar binding sites.
L Stryer
Journal of molecular biology, 13(2), 482-495 (1965-09-01)

Cikkek

Nitric oxide (NO) as a signal transporter in neurons, endothelial cells and in the immune system.

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