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Hybridization indicator

CNTs can also be used as hybridization indicators with amplifying properties as demonstrated by Wang and coworkers [164—166]. They showed that CNTs can play a dual amplification role in both the recognition and transduction events, namely as... [Pg.154]

The 100% incidence in the large bowel of Fj and susceptible backcross hybrids indicated dominance of the ICR-derived susceptibility to carcinogenesis by 1,2-dimethylhydrazine. Findings in the F2 and resistant backcross hybrids are mutually supportive and in agreement with the respective 75% and 50% tumour incidences expected if a single dominant susceptibility gene is inherited from the ICR grandparent (Evans et al., 1977). [Pg.971]

We can use the generalized expression for hybrids to find the relation between hybridization indices and angle between two hybrids xi and X2 (Equations A1.10). Since the expressions in braces are equivalent to ordinary three-dimensional vectors of unit length, the three-dimensional vector dot product, found by... [Pg.47]

K.M. Millan and S.K. Mikkelsen, Sequence-selective biosensor for DNA based on electroactive hybridization indicators, Anal. Chem., 65 (1993) 2317-2323. [Pg.463]

A. Erdem, K. Kerman, B. Meric and M. Ozsoz, Methylene blue as a novel electrochemical hybridization indicator, Electroanalysis, 13 (2001) 219-223. [Pg.463]

Hume DA, Monkley SJ, Wainwright BJ. Detection of c-fms protooncogene in early mouse embryos by whole mount in situ hybridization indicates roles for macrophages in tissue remodelling. British Journal of Haematology 1995, 90, 939-942. [Pg.52]

More recent calculations, however, which allow for more spd hybridization indicate a preference for three-dimensional structures.31 The new calculations show the delicate balance between the various geometries. Calculations for... [Pg.155]

To confirm that hi, hi, and hs are equivalent to each other, we can calculate their hybridization indices and see that they are identical. The hybridization index n of a hybrid orbital is defined as... [Pg.105]

The development of a biosensor capable of selectively detecting a point mutation in human DNA would enable an early diagnosis of inherited human diseases. With this aim, a prototype of a sequence-selective DNA biosensor based on hybridization indicators was evaluated [90]. For the covalent immobilization of single-stranded DNA onto the carboxylic groups present on the surfaces of oxidized glassy carbon, water-soluble carbodiimide and /V-hydroxysuccinimide coupling reagents were used. [Pg.109]

In this case, the duplex formation is commonly detected in connection with the use of appropriate electroactive hybridization indicators such as cationic metal complexes (Co(phen)33+, Co(bpy)33+, [Cu(phen)2]2+, Ru(bpy)32+ among others [18-22,32]), or organic compounds (anthracyclines, phenoth-iazine, etc. [15,24,25,28,29]). These compounds interact in different ways with ss- or dsDNA but preferentially with dsDNA undergoing reversible... [Pg.36]

Of considerable further interest is the finding of Marmur and Ts o (1961) that the denaturation of DNA in formamide-water mixtures results in the separation of the two polynucleotide strands. An N N hybrid Escherichia coli DNA was treated with 95% formamide at 37°C for 15 min at an ionic strength of 0.01, the formamide was then removed by dialysis, and the DNA was centrifuged in a CsCl density gradient. The presence of two bands of density different from that of the original hybrid indicates that strand separation occurred. It is of considerable practical interest that these conditions are much milder than those required to achieve strand separation in aqueous solution. Whether strand separation occurs also in solutions of DNA in other nonaqueous solvents is not yet determined. [Pg.55]

Double bond position. Stracture A has a C-O double bond, whereas structure B has a C-N double bond. A dashed line in the hybrid indicates partial double bond character between these atoms. [Pg.24]

The resonance description of benzene matches the Kekule description with one important exception. The two Kekule representations are not in equilibrium witb each other. Instead, the true structure of benzene is a resonance hybrid of the two Lewis structures, with the dashed lines of the hybrid indicating the position of the 7i bonds. [Pg.608]

Electrochemical biosensing of DNA sequences using direct electrochemical detection of DNA hybridization, adsorptive striping analysis, metal complex hybridization indicators, organic compound electroactive hybridization indicators and renewable DNA probes have been considered [65,67,72,73]. With metal complexes and organic compound electroactive hybridization indicators, non-specific adsorption can influence the results [68,94]. Chrono-potentiometric detection was used to monitor the hybridization onto screen-printed carbon electrodes by following the oxidation of the guanine peak, which decreases in the presence of the complementary strand [64,68,73]. [Pg.400]

Enzyme DNA hybridization assays with electrochemical detection can offer enhanced sensitivity and reduced instrumentation costs in comparison with their optical counterparts. Efforts to prevent non-specific binding of the codissolved enzyme and to avoid fouling problems by selecting conditions suitable to amplify the electrode response have been reported by Heller and co-workers [107]. A disposable electrochemical sensor based on an ion-exchange film-coated screen-printed electrode was described by Limoges and co-workers for an enzyme nucleic acid hybridization assay using alkaline phosphatase [108] or horseradish peroxidase [109]. In another methodology to improve sensitivity, a carbon paste electrode with an immobilized nucleotide on the electrode surface and methylene blue as hybridization indicator was coupled, by Mascini and co-workers [110], with PGR amplification of DNA extracted from human blood for the electrochemical detection of virus. [Pg.401]

A six-membered cyclic conjugated triene system is called an aromatic ring. The individual single and double bonds are shown in individual canonical structures, while the resonance hybrid indicates the delocalisation that takes place in reality. [Pg.52]

Also shown in table 4.01 are a number of examples of metallic elements which have been found experimentally to adopt the states of hybridization indicated. It will be seen that for these elements the valency state has been quoted the reason for this will be made clear when we come later to consider the crystal structures of some of the compounds of these elements in detail. At this point, however, we may draw attention to the fact that some elements (e.g. Ni11) can occur in several alternative states of hybridization, some (e.g. PtXI) are found only in one, and for some the state of hybridization depends on the valency (e.g. Cu11 is always dsp2, Cu1 may be sp or spz hybridized). [Pg.61]

An sp d hybridization indicates that the electron-pair arrangement about iodine is trigonal bipyramidal. If four fluorines are placed around iodine, the total number of valence electrons is 35. Only 34 electrons are required to complete a trigonal bipyramidal electron-pair arrangement with four bonds and one lone pair of electrons. Taking one valence electron away gives the cation, IF4. ... [Pg.277]

The long-range electron transfer reactions in ruthenium-modified myoglobin, in which the labile heme unit has been replaced by various metalloporphyrins, have been reviewed. The reductions of the [Ru(NH3)5] moiety, attached at His-48, by Pd- and Pt-substituted hemes in myoglobin proceed at rates of 9 1 x 1(P and 1.2x lO s", respectively. The difference in rates for electron transfer between Fe (heme) and Mg or Zn(porphyrin) centers in [a(Fe(II)P),j3(M T)] hemoglobin hybrids indicates a direct process as opposed to the involvement of a conformational gate. Using [Co(NH3)5Cl] to quench the Zn state, a rate constant of 2.4 x 10 s has been measured for back electron transfer within [a(Zn- -P)i8(Fe(III)CN)]. ... [Pg.39]


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See also in sourсe #XX -- [ Pg.316 ]




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