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Matrix Multiplexing

Depending on the food matrix, multiplex DNA can show some discrepancies in the detection of different allergenic targets, due to differential efficiency of the amplification process. This issue has been shown in the case of the determination of the hazelnut allergen isoforms Cor a 1.03 and Cor a 1.04 in some matrices, including dark chocolate, soy milk, lecithin supplement, and snack muesli (Bettazzi et al., 2008). For this reason, multiplex assays must be evaluated carefully during and after development, to reduce inconsistent results. [Pg.192]

Yang, L. et al. 2001. Evaluation of a four-channel multiplexed electrospray triple quadrupole mass spectrometer for the simultaneous validation of LC/MS/MS methods in four different preclinical matrixes. Anal. Chem. 73 1740. [Pg.243]

An approach to multiplexing analysis was presented by Min et al. [23], who de-velopped a SAMDI-based assay scheme to screen for the activity of different kinases. In this assay scheme, peptide substrates were used that are specific for one type of kinase. A mixture of four substrates was immobilized on the SAM. After incubation with an appropriate kinase, the target surface was rinsed, thus stopping the reaction. Matrix was deposited on the surface and MALDI-MS analysis was carried out (Fig. 8.13). By monitoring the signal intensities for the substrates... [Pg.297]

Fig. 8.13 A multiplexing SAMDI-MS assay. In this case, a mixture of three substrates is immobilized on the SAM. After incubation with appropriate enzyme solutions, the enzymatic reaction is quenched by rinsing the surface. Subsequently, matrix is deposited on the surface and MALDI-MS is carried out. Consumption of all three substrates can thus be determined in parallel. Fig. 8.13 A multiplexing SAMDI-MS assay. In this case, a mixture of three substrates is immobilized on the SAM. After incubation with appropriate enzyme solutions, the enzymatic reaction is quenched by rinsing the surface. Subsequently, matrix is deposited on the surface and MALDI-MS is carried out. Consumption of all three substrates can thus be determined in parallel.
To produce display panels it is necessary to address a large array of pixels. This can be achieved in two basic ways, either by multiplexing or by using a matrix arrangement of transistors. [Pg.307]

It can be safely predicted that applications of liquid crystals will expand in the future to more and more sophisticated areas of electronics. Potential applications of ferroelectric liquid crystals (e.g. fast shutters, complex multiplexed displays) are particularly exciting. The only LC that can show ferroelectric property is the chiral smectic C. Viable ferroelectric displays have however not yet materialized. Antifer-roelectric phases may also have good potential in display applications. Supertwisted nematic displays of twist artgles of around 240° and materials with low viscosity which respond relatively fast, have found considerable application. Another development is the polymer dispersed liquid crystal display in which small nematic droplets ( 2 gm in diameter) are formed in a polymer matrix. Liquid crystalline elastomers with novel physical properties would have many applications. [Pg.465]

In general, it is easier (and faster) to develop an HPLC-ESI-MS/MS method for multiple analytes with the matrix effects identified and under control as compared to IA (see below). Furthermore, selectivity and interference from matrix components and/or metabolites is less of a problem with an LC-MS/MS method compared to IA. With an appropriate internal standard (IS), LC-MS/MS methods are more precise than IA. Moreover, the LC-MS/MS calibration range is broader and can accommodate disproportionate concentration ranges of the drug compound and its metabolites. In contrast, most IA are geared to quantify only one analyte at a time because the method development of multiplex IA is complicated and often cannot be optimized for all analytes of interest. [Pg.162]

An advantage of the ASO method is that it can be used to simultaneously test samples for several different mutations by the use of multiple probes bound to a solid matrix. In practice, the success of this method relies on precisely establishing conditions for optimal oligonucleotide hybridization in order to ensure specific probe hybridization, and so multiplex ASO assays can be difficult to develop. Molecular diagnostic kits for use in genetic disorders based on ASO methods are available (14). [Pg.316]

PubMatrix is a simple way to rapidly and systematically compare any list of terms against any other list of terms in PubMed. It reports back the frequency of co-occurrence between all pairwise comparisons between the two lists as a matrix table. It allows the user to build up tables of words in the context of experiments. This is useful for analyzing combinatorial datasets such as cDNA microarrays, genomic, proteomic, or other multiplex comparisons. [Pg.500]

Various matrix addressing schemes are possible with two- and three-terminal devices. For more information, the reader is referred to an early paper of the RCA group (Lechner et al., 1971). Matrix addressing differs from multiplexing in that the LC can be driven at 100% duty factor, maintaining superior optical performance. [Pg.120]

Spiropyrans show promise for optical recording, three-dimensional optical memories,214 and holography.215 The dyes currently under study for these applications very probably will not be used merely dissolved in a bulk polymer matrix, but will be oriented in films and membranes, or adsorbed or vapor deposited on solid substrates to take advantage of the nonlinear optical properties of the colored forms. For example, thick (0.5 mm) PMMA films of 6-nitro-thiaBIPS can be used to record wavelength-multiplexed volume holograms with an infrared diode laser. This system is impractical at present because of fatigue and poor diffraction efficiencies.216... [Pg.67]

Direct, multiplex and active matrix addressing are the three electronic drive methods used to generate the appropriate voltage at a particular pixel of an LCD, see Figures 2.11-2.14. The size, shape and pattern of electrodes on LCD substrates are fashioned to be compatible with the chosen method of addressing. In directly addressed LCDs the desired pattern of pixel electrodes is created by etching on one surface. A non-pattemed back electrode on the second surface provides the electrical contact. LCDs with multiplexed addres-... [Pg.28]

The requirement of a very high and constant resistivity over time of nematic mixtures for TN-LCDs with active matrix addressing meant that new liquid crystals which met this and the other specifications, such as low viscosity and high positive dielectric anisotropy, were needed. The nitriles used in nematic mixtures for TN-LCDs with direct or multiplex addressing were soon found to be unsuitable for TN-LCDs with active matrix addressing. The polar nature of the cyano group leads to the solvation of ions from some of the layers on the... [Pg.81]

OLEDs can be addressed in a similar fashion to LCDs, see Chapter 2, i.e. directly with segmented electrodes, see Figure 4.8, by multiplexed addressing with rows and columns of electrode strips, see Figure 4.9 and by active matrix addressing with one transistor at each pixel, see Figure 4.10. The major... [Pg.143]


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See also in sourсe #XX -- [ Pg.23 , Pg.61 , Pg.79 , Pg.153 , Pg.205 , Pg.211 , Pg.214 ]




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