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Signal quenching

The process of RGS recruitment to the membrane-bound receptor, however, seems to be constitutive—it appears to be independent of the state of activation of the receptor or G protein. This recruitment may facilitate signal quenching because the combination of 30 RGS proteins and 20 Ga subunits allows for a diverse pattern of inactivation. RGS proteins, therefore, are recruited to the plasma membrane in cells expressing either Ga subunits (Gsa) or linked GPCRs (e.g., Dj-dopamine receptor) in preparation for the GAP activity that quenches G protein signaling (104,105). [Pg.88]

Signal quenched before amplHicatiDn Signal increase ater incerporalion... [Pg.1438]

The detector is extremely sensitive to temperature and flow changes as well as the Hj/02 ratio in the fuel-rich flame. Deactivation of the excited species by collision with organic radicals can cause signal quenching when high hydrocarbon concentrations co-elute. [Pg.138]

Practical aspects. Chemiluminescence detectors are only applicable as GC detectors because of signal quenching by high hydrocarbon levels such as solvents used as mobile phases in LC. They are primarily used for selective sulfur detection. [Pg.138]

Fluorescence spectrophotometry Measurement of fluorescence signal quenching of an active-site tryptophan as a function of ligand binding described as AF = AF, x-Kd(AF/[L]) FKBP [5]... [Pg.90]

In addition to the use of emittive acceptors to measure sensitized emission, various nonemitting compounds have also been used in assays where the proximity creates signal quenching. Those assays are mainly apphed in enzymatic assays where hydrolysis intermpts the proximity and reaction is followed by recovery of the signal. [Pg.365]

For detecting and percentage evaluation of the participation of the amount of austenite in the quenched structure of hyper-eutectoidal steel, devices manufactured by CMP type WIROTEST 202 and WIROTEST 12 finish (Table 1.) are applied. These devices allow to detea and evaluate the content of residual austenite as well as form the signal for part segregation with austenite content above the allowed amount, as well as parts with grinding burning... [Pg.21]

In the equation, the subscripts 1 and 2 refer to the reference compound and the compound of interest, respectively, is the intensity of the fluorescent signal of each compound measured as peak height in centimeters, 8 is the molar absorptivity, c is the concentration in moles per liter, and is the fluorescence quantum yield. In this application, i is set at 1.00. The concentrations of the solutions that were tested ranged from 10 to 10 M. The solutions run at the higher concentrations were all checked for self-quenching, but none was found. All measurements, except the fluorescence-versus-solvent study, were made in 0.1-N phosphate buffer, pH 7.4. Slit settings on the Perkin-Elmer MPF-2A were 10 mp (nm) for both emission and excitation monochromators. [Pg.221]

Fig. 3a, b. Schematic representation of (a) conventional fluorescent sensor and (b) fluorescent sensor with signal amplification. Open rhombi indicate coordination sites and black rhombi indicate metal ions. The curved arrows represent quenching processes. In the case of a den-drimer, the absorbed photon excites a single fluorophore component, which is quenched by the metal ion regardless of its position... [Pg.187]

It has been demonstrated that dendrimers can be used also as fluorescent sensors for metal ions. Poly(propylene amine) dendrimers functionalized with dansyl units at the periphery like 34 can coordinate metal ions by the aliphatic amine units contained in the interior of the dendrimer [80]. The advantage of a dendrimer for this kind of application is related to the fact that a single analyte can interact with a great number of fluorescent units, which results in signal amplification. For example, when a Co ion enters dendrimer 34, the fluorescence of all the 32 dansyl units is quenched with a 32-fold increase in sensitivity with respect to a normal dansyl sensor. This concept is illustrated in Fig. 3. [Pg.187]

Obviously, only parts of the defects created on the surface are paramagnetic, and thus EPR active. Nonetheless subsequent XiCl4 deposition on samples covered with a non-epitaxial MgCl2 film quenches the EPR signal by 40% [21], This can be taken as a clear indication that some of the defects are localized on the surface of the MgCl2 film, while most of the defects are bulk defects not influenced by adsorbed TiCl4. [Pg.134]


See other pages where Signal quenching is mentioned: [Pg.360]    [Pg.14]    [Pg.291]    [Pg.200]    [Pg.327]    [Pg.179]    [Pg.133]    [Pg.505]    [Pg.136]    [Pg.557]    [Pg.291]    [Pg.424]    [Pg.360]    [Pg.14]    [Pg.291]    [Pg.200]    [Pg.327]    [Pg.179]    [Pg.133]    [Pg.505]    [Pg.136]    [Pg.557]    [Pg.291]    [Pg.424]    [Pg.799]    [Pg.1206]    [Pg.2116]    [Pg.634]    [Pg.319]    [Pg.747]    [Pg.139]    [Pg.375]    [Pg.453]    [Pg.455]    [Pg.585]    [Pg.585]    [Pg.1204]    [Pg.108]    [Pg.15]    [Pg.16]    [Pg.25]    [Pg.233]    [Pg.159]    [Pg.161]    [Pg.170]    [Pg.207]    [Pg.286]    [Pg.173]    [Pg.38]    [Pg.63]    [Pg.213]   


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