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Formal Name 4,4'-bis(phenylamino)- [1,1'-binaphthalene]-5,5'-disulfonic acid, dipotassium salt CAS Number 912-60-7 Synonyms 4,4'-Dianilino-1,1'-binaphthyl-5,5'-disulfonic Acid Molecular Formula C32H22N2O6S2 • 2K Formula Weight 672.9 Purity
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Bis-ANS is a fluorescent probe for nonpolar cavities in proteins. Used to detect A β fibre (K d = ~80 nM); exhibits distinct fluorescent profiles for fibres and oligomers. Fluoresces in hydrophobic environments, negligible fluorescence in water solutions. Excitation\emission λ ~ 355\520 nm at pH 7.4.
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5,5'-Bis [8- (phenylamino)-1-naphthalenesulfonate] (bis-ANS), the fluorescent probe which binds to tubulin, inhibits its assembly into microtubules [Horowitz et al. (1984) J. Biol. Chem. 259, 14647-14650].
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Bis-ANS is superior to 1-8-ANS as a probe for nonpolar cavities in proteins, often binding with an affinity that is orders-of-magnitude higher. Anilinonaphthalene sulfonates Invitrogen Bis-ANS (4,4'-Dianilino-1,1'-Binaphthyl-5,5'-Disulfonic Acid, | Fisher Scientific
BisANS induces LLPS of the TDP43 LCD a Chemical structure of
compound Summary 4,4'-Dianilino-1,1'-binaphthyl-5,5'-disulfonic acid dipotassium salt PubChem CID 16213473 Structure Chemical Safety Laboratory Chemical Safety Summary (LCSS) Datasheet Molecular Formula C32H22K2N2O6S2 Synonyms Bis-ans 65664-81-5 4,4'-Dianilino-1,1'-binaphthyl-5,5'-disulfonic acid dipotassium salt Bis-ANS (dipotassium)
Threedimensional structure of bisANS. For clarity only polar
Background and objective: Published algorithms for classification of human sperm heads are based on relatively small image databases that are not open to the public, and thus no direct comparison is available for competing methods. We describe a gold-standard for morphological sperm analysis (SCIAN-MorphoSpermGS), a dataset of sperm head images with expert-classification labels in one of the.
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open access Highlights • Fluorescence-based assay is a fast and easy tool for detection of RNA-IFIT binding. • Bis-ANS probe demonstrates effective binding to the IFIT proteins. • Bis-ANS is located inside the RNA binding tunnel of the IFIT proteins. • Developed assay enables binding studies at low RNA concentrations. Abstract Keywords IFIT
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Bis-ANS exhibits a chaperone-like activity, effectively suppressing protein aggregation and preventing a certain degree of heat-inactivation of enzymes [5]. Horowitz et al. have recently shown that bis-ANS binds to tubulin, inhibiting the formation of microtubules [2], [11]. Their experiments demonstrate the presence of more than one site for.
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Bis-ANS is a fluorescent probe for nonpolar cavities in proteins. Used to detect A β fibre (K d = ~80 nM); exhibits distinct fluorescent profiles for fibres and oligomers. Fluoresces in hydrophobic environments, negligible fluorescence in water solutions. Excitation\emission λ ~ 355\520 nm at pH 7.4. Also modulates liquid-liquid phase.
Titration of bisANS binding. Binding of bisANS to G protein (A and B
bis-ANS is a high-affinity non-covalent extrinsic fluorescent dye used to analyze protein conformation.1 Its predominant interaction with proteins is through its hydrophobic phenyl and naphthyl rings.2 bis-ANS has an excitation maxima of 390 nm.3 It has an emission maximum of 523 nm when free in solution but
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Product Overview Documents Bis-ANS is superior to 1-8-ANS as a probe for nonpolar cavities in proteins, often binding with an affinity that is orders-of-magnitude higher. Anilinonaphthalene sulfonates (ANS) are essentially nonfluorescent in water, only becoming appreciably fluorescent when bound to membranes.
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ANS has the potential to characterize proteins in solid states. • ANS fluorescence in protein films reveals the hydrophobic sites with distinct properties. • Short lifetime DAS of ANS in hydrated protein films is similar to that of ANS-protein complexes in solution. •
(A) Change of bisANS fluorescence intensity (fluorescence maximum, λ
These results resemble effects of bis-ANS on BSA, where low ratios of bis-ANS:protein were found to increase thermostability of BSA, while higher ratios induced transition of the protein into a molten globule-like state (Celej et al. 2003). Therefore, we propose that accelerated aggregation of IL-1ra in the presence of 4.2-21 mM ANS reflects.
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Depending on context, bis-ANS can both induce LLPS de novo as well as prevent formation of homotypic liquid droplets. Our study also reveals the mechanisms by which bis-ANS and related.
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Despite emergence of bis-ANS as a major fluorescence probe of proteins structure, conformational and spectroscopic properties of protein/bis-ANS complexes remains largely unexplored. We have shown that fluorescence polarization of both ANS and bis-ANS is excitation wavelength dependent and this is a property of all protein-ANS/bis-ANS complexes.
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Bis-ANS is a fluorescent probe for nonpolar cavities in proteins. Used to detect A β fibre (K d = ~80 nM); exhibits distinct fluorescent profiles for fibres and oligomers. Fluoresces in hydrophobic environments, negligible fluorescence in water solutions. Excitation\emission λ ~ 355\520 nm at pH 7.4.