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Introduction fluorescence

Biomolecules Analysis Introduction Fluorescence-based Biosensors... [Pg.21]

Protein adsorption has been studied with a variety of techniques such as ellipsome-try [107,108], ESCA [109], surface forces measurements [102], total internal reflection fluorescence (TIRE) [103,110], electron microscopy [111], and electrokinetic measurement of latex particles [112,113] and capillaries [114], The TIRE technique has recently been adapted to observe surface diffusion [106] and orientation [IIS] in adsorbed layers. These experiments point toward the significant influence of the protein-surface interaction on the adsorption characteristics [105,108,110]. A very important interaction is due to the hydrophobic interaction between parts of the protein and polymeric surfaces [18], although often electrostatic interactions are also influential [ 116]. Protein desorption can be affected by altering the pH [117] or by the introduction of a complexing agent [118]. [Pg.404]

Sensitivity levels more typical of kinetic studies are of the order of lO molecules cm . A schematic diagram of an apparatus for kinetic LIF measurements is shown in figure C3.I.8. A limitation of this approach is that only relative concentrations are easily measured, in contrast to absorjDtion measurements, which yield absolute concentrations. Another important limitation is that not all molecules have measurable fluorescence, as radiationless transitions can be the dominant decay route for electronic excitation in polyatomic molecules. However, the latter situation can also be an advantage in complex molecules, such as proteins, where a lack of background fluorescence allow s the selective introduction of fluorescent chromophores as probes for kinetic studies. (Tryptophan is the only strongly fluorescent amino acid naturally present in proteins, for instance.)... [Pg.2958]

EPA Method 6C is the instrumental analyzer procedure used to determine sulfur dioxide emissions from stationaiy sources (see Fig. 25-30). An integrated continuous gas sample is extracted from the test location, and a portion of the sample is conveyed to an instrumental analyzer for determination of SO9 gas concentration using an ultraviolet ( UV), nondispersive infrared (NDIR), or fluorescence analyzer. The sample gas is conditioned prior to introduction to the gas analyzer by removing particulate matter and moisture. Sampling is conducted at a constant rate for the entire test rim. [Pg.2200]

As atomic fluorescence spectrometer a mercury analyzer Mercur , (Analytik-Jena, Germany) was used. In the amalgamation mode an increase of sensitivity by a factor of approximately 7-8 is obtained compared with direct introduction, resulting in a detection limit of 0,09 ng/1. This detection limit has been improved further by pre-concentration of larger volumes of samples and optimization of instrumental parameters. Detection limit 0,02 ng/1 was achieved, RSD = 1-6 %. [Pg.171]

A nano-light-source generated on the metallic nano-tip induces a variety of optical phenomena in a nano-volume. Hence, nano-analysis, nano-identification and nanoimaging are achieved by combining the near-field technique with many kinds of spectroscopy. The use of a metallic nano-tip applied to nanoscale spectroscopy, for example, Raman spectroscopy [9], two-photon fluorescence spectroscopy [13] and infrared absorption spectroscopy [14], was reported in 1999. We have incorporated Raman spectroscopy with tip-enhanced near-field microscopy for the direct observation of molecules. In this section, we will give a brief introduction to Raman spectroscopy and demonstrate our experimental nano-Raman spectroscopy and imaging results. Furthermore, we will describe the improvement of spatial resolution... [Pg.24]

New applications (e.g. demand for fluorescent, pearlescent and other brilliant pigments introduction of photoconductive elements in polymer-based electro-optical devices)... [Pg.716]

The nondestructive introduction of a fluorescent label would provide the molecule with a nonradioactive fluorophore, yet would preserve the option for direct radiolabelling of the fluorescent moiety with 125Iodine. This approach was pioneered by Nagasawa et al. (5) who reacted native or /V-desulfated heparins with a fluorescein isothiocyanate (FITC). The resulting degree of labelling was low... [Pg.62]

Demchenko AP (2009) Introduction to fluorescence sensing. Springer, Amsterdam... [Pg.22]

On the other hand, the introduction of halide substituents at the C-2 and C-6 position decreases fluorescence quantum yields and gives a bathochromic shift of emission maxima. For example, bromine at the C-2 and C-6 position in compound 14b deteriorates fluorescence quantum yields from 0.95 (14a) to 0.45 and the emission maximum is red-shifted by 42 nm. Moreover, iodine at the C-2,6 position in compound 14d gives the similar bathochromic shift to bromine (14b, 44 nm) and more dramatic reduction in quantum yields (almost nonfluorescent, photophysical properties were interpreted as the heavy atom effect of halides on a BODIPY core skeleton. The bathochromic shift of BODIPY dyes without dramatic decrease in quantum yield was observed by the introduction of vinyl substituents at the C-2 and C-6 position. The extension of conjugation... [Pg.165]

The C-3 and C-5 position of BODIPY core skeleton is one of the most important points for the substitution to tune photophysical properties, including absorption and/or emission maxima as well as fluorescence quantum yields. First of all, the introduction of amine-based (15d-15g) or sulfur-based (15b-15c) nucleophiles can... [Pg.166]

As shown in Fig. 25b, the systematic tuning of emission wavelength was achieved by the combinatorial introduction of substitutents at the two diversity points on the fluorescent core skeleton. In addition to the synthetic versatility and predictability on emission wavelengths, these novel fluorophores were compatible with the modification of biopolymers and successfully applied in the immunofluorescence (see Fig. 25c). [Pg.178]


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See also in sourсe #XX -- [ Pg.262 ]




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